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nsv5954917

  • 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: 81 SVs from 13 studies. See in: genome view    
Submitted genomic161,416,696-161,416,696Question Mark
Overlapping variant regions from other studies: 81 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):160,843,702-160,843,702Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5954917Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5161,416,696161,416,696
nsv5954917RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5160,843,702160,843,702

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17413866insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17413866Submitted genomicNC_000005.10:g.161
416696_161416697in
s252
GRCh38 (hg38)NC_000005.10Chr5161,416,696161,416,696
nssv17413866RemappedPerfectNC_000005.9:g.1608
43702_160843703ins
252
GRCh37.p13First PassNC_000005.9Chr5160,843,702160,843,702

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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