esv1011742

  • Variant Calls:1
  • 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: 64 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):29,540,983-29,540,983Question Mark
Overlapping variant regions from other studies: 64 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):29,580,599-29,580,599Question Mark
Overlapping variant regions from other studies: 29 SVs from 9 studies. See in: genome view    
Submitted genomic29,547,124-29,547,124Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv1011742RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000007.14Chr729,540,98329,540,983
esv1011742RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000007.13Chr729,580,59929,580,599
esv1011742Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr729,547,12429,547,124

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisZygosityOther Calls in this Sample and Study
essv4362822insertionHuRefSequencingSequence alignmentHomozygous780,358

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv4362822RemappedPerfectNC_000007.14:g.295
40982_29540983insA
TA
GRCh38 (hg38)First PassNC_000007.14Chr729,540,98329,540,983
essv4362822RemappedPerfectNC_000007.13:g.295
80598_29580599insA
TA
GRCh37 (hg19)First PassNC_000007.13Chr729,580,59929,580,599
essv4362822Submitted genomicNC_000007.12:g.295
47123_29547124insA
TA
NCBI36 (hg18)NC_000007.12Chr729,547,12429,547,124

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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