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nsv5892076

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 210 SVs from 35 studies. See in: genome view    
Submitted genomic115,581,315-115,616,316Question Mark
Overlapping variant regions from other studies: 210 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):114,917,012-114,952,013Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5892076Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5115,581,315115,616,316
nsv5892076RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5114,917,012114,952,013

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17423099deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17423099Submitted genomicNC_000005.10:g.115
581315_115616316de
l
GRCh38 (hg38)NC_000005.10Chr5115,581,315115,616,316
nssv17423099RemappedPerfectNC_000005.9:g.1149
17012_114952013del
GRCh37.p13First PassNC_000005.9Chr5114,917,012114,952,013

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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