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nsv6197691

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 25 studies. See in: genome view    
Submitted genomic38,371,489-38,371,548Question Mark
Overlapping variant regions from other studies: 11 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):154,760-154,819Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6197691Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1738,371,48938,371,548
nsv6197691RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315948.2Chr17|NW_0
03315948.2
154,760154,819

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17938462deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17938462Submitted genomicNC_000017.11:g.383
71489_38371548del
GRCh38 (hg38)NC_000017.11Chr1738,371,48938,371,548
nssv17938462RemappedPerfectNW_003315948.2:g.1
54760_154819del
GRCh37.p13First PassNW_003315948.2Chr17|NW_0
03315948.2
154,760154,819

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)
nssv179384620.89919882212
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