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nsv5521656

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 80 SVs from 23 studies. See in: genome view    
Submitted genomic8,236,270-8,236,326Question Mark
Overlapping variant regions from other studies: 80 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):8,301,154-8,301,210Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521656Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr198,236,2708,236,326
nsv5521656RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr198,301,1548,301,210

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721124deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721124Submitted genomicNC_000019.10:g.823
6270_8236326del
GRCh38 (hg38)NC_000019.10Chr198,236,2708,236,326
nssv17721124RemappedPerfectNC_000019.9:g.8301
154_8301210del
GRCh37.p13First PassNC_000019.9Chr198,301,1548,301,210

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)
nssv17721124<0.00116404
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