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nsv5519011

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69,667

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 368 SVs from 45 studies. See in: genome view    
Submitted genomic39,916,896-39,986,562Question Mark
Overlapping variant regions from other studies: 366 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):38,073,149-38,142,815Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5519011Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1739,916,89639,986,562
nsv5519011RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1738,073,14938,142,815

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713066duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713066Submitted genomicNC_000017.11:g.399
16896_39986562dup
GRCh38 (hg38)NC_000017.11Chr1739,916,89639,986,562
nssv17713066RemappedPerfectNC_000017.10:g.380
73149_38142815dup
GRCh37.p13First PassNC_000017.10Chr1738,073,14938,142,815

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)
nssv17713066<0.00116404
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