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esv3890509

  • Variant Calls:7
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 449 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):155,762,658-155,762,658Question Mark
Overlapping variant regions from other studies: 445 SVs from 24 studies. See in: genome view    
Submitted genomic154,992,320-154,992,320Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3890509RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX155,762,658155,762,658
esv3890509Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000023.10ChrX154,992,320154,992,320

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv25752961alu insertionHG02284SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous4,143
essv25752962alu insertionHG02485SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,523
essv25752963alu insertionHG02982SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous4,258
essv25752964alu insertionHG03189SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,973
essv25752965alu insertionNA18873SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous4,059
essv25752966alu insertionNA19037SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,920
essv25752967alu insertionNA19102SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mappingHeterozygous3,889

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv25752961RemappedPerfectNC_000023.11:g.155
762658_155762659in
s276
GRCh38.p12First PassNC_000023.11ChrX155,762,658155,762,658
essv25752962RemappedPerfectNC_000023.11:g.155
762658_155762659in
s276
GRCh38.p12First PassNC_000023.11ChrX155,762,658155,762,658
essv25752963RemappedPerfectNC_000023.11:g.155
762658_155762659in
s276
GRCh38.p12First PassNC_000023.11ChrX155,762,658155,762,658
essv25752964RemappedPerfectNC_000023.11:g.155
762658_155762659in
s276
GRCh38.p12First PassNC_000023.11ChrX155,762,658155,762,658
essv25752965RemappedPerfectNC_000023.11:g.155
762658_155762659in
s276
GRCh38.p12First PassNC_000023.11ChrX155,762,658155,762,658
essv25752966RemappedPerfectNC_000023.11:g.155
762658_155762659in
s276
GRCh38.p12First PassNC_000023.11ChrX155,762,658155,762,658
essv25752967RemappedPerfectNC_000023.11:g.155
762658_155762659in
s276
GRCh38.p12First PassNC_000023.11ChrX155,762,658155,762,658
essv25752961Submitted genomicNC_000023.10:g.154
992320_154992321in
s276
GRCh37 (hg19)NC_000023.10ChrX154,992,320154,992,320
essv25752962Submitted genomicNC_000023.10:g.154
992320_154992321in
s276
GRCh37 (hg19)NC_000023.10ChrX154,992,320154,992,320
essv25752963Submitted genomicNC_000023.10:g.154
992320_154992321in
s276
GRCh37 (hg19)NC_000023.10ChrX154,992,320154,992,320
essv25752964Submitted genomicNC_000023.10:g.154
992320_154992321in
s276
GRCh37 (hg19)NC_000023.10ChrX154,992,320154,992,320
essv25752965Submitted genomicNC_000023.10:g.154
992320_154992321in
s276
GRCh37 (hg19)NC_000023.10ChrX154,992,320154,992,320
essv25752966Submitted genomicNC_000023.10:g.154
992320_154992321in
s276
GRCh37 (hg19)NC_000023.10ChrX154,992,320154,992,320
essv25752967Submitted genomicNC_000023.10:g.154
992320_154992321in
s276
GRCh37 (hg19)NC_000023.10ChrX154,992,320154,992,320

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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