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nsv5500724

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,597

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 29 studies. See in: genome view    
Submitted genomic22,612,378-22,614,974Question Mark
Overlapping variant regions from other studies: 87 SVs from 29 studies. See in: genome view    
Remapped(Score: Good):23,081,284-23,083,877Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500724Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1422,612,37822,614,974
nsv5500724RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1423,081,28423,083,877

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17693914deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17693914Submitted genomicNC_000014.9:g.2261
2378_22614974del
GRCh38 (hg38)NC_000014.9Chr1422,612,37822,614,974
nssv17693914RemappedGoodNC_000014.8:g.2308
1284_23083877del
GRCh37.p13First PassNC_000014.8Chr1423,081,28423,083,877

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17693914<0.00136404
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