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nsv4634386

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,987

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 338 SVs from 36 studies. See in: genome view    
Remapped(Score: Good):149,722,190-149,750,176Question Mark
Overlapping variant regions from other studies: 328 SVs from 33 studies. See in: genome view    
Submitted genomic148,803,850-148,831,837Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4634386RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX149,722,190149,750,176
nsv4634386Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000023.10ChrX148,803,850148,831,837

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16183118deletionCuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16183118RemappedGoodNC_000023.11:g.149
722190_149750176de
l
GRCh38.p12First PassNC_000023.11ChrX149,722,190149,750,176
nssv16183118Submitted genomicNC_000023.10:g.148
803850_148831837de
l
GRCh37 (hg19)NC_000023.10ChrX148,803,850148,831,837

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv161831180.04472542
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