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nsv5517916

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:126,021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 651 SVs from 73 studies. See in: genome view    
Submitted genomic36,435,980-36,562,000Question Mark
Overlapping variant regions from other studies: 386 SVs from 44 studies. See in: genome view    
Remapped(Score: Pass):320,732-429,138Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517916Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,435,98036,562,000
nsv5517916RemappedPassGRCh37.p13PATCHESFirst PassNW_003315949.1Chr17|NW_0
03315949.1
320,732429,138

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712861duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712861Submitted genomicNC_000017.11:g.364
35980_36562000dup
GRCh38 (hg38)NC_000017.11Chr1736,435,98036,562,000
nssv17712861RemappedPassNW_003315949.1:g.3
20732_429138dup
GRCh37.p13First PassNW_003315949.1Chr17|NW_0
03315949.1
320,732429,138

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)
nssv177128610.002146398
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