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nsv5620509

  • 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: 144 SVs from 39 studies. See in: genome view    
Submitted genomic113,603,758-113,603,758Question Mark
Overlapping variant regions from other studies: 144 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):114,361,335-114,361,335Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5620509Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2113,603,758113,603,758
nsv5620509RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2114,361,335114,361,335

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17107879insertionHG00512SequencingSequence alignment6,637

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17107879Submitted genomicNC_000002.12:g.113
603758_113603759in
s440
GRCh38 (hg38)NC_000002.12Chr2113,603,758113,603,758
nssv17107879RemappedPerfectNC_000002.11:g.114
361335_114361336in
s440
GRCh37.p13First PassNC_000002.11Chr2114,361,335114,361,335

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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