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nsv5941616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,321

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1757 SVs from 101 studies. See in: genome view    
Submitted genomic36,083,984-36,190,304Question Mark
Overlapping variant regions from other studies: 716 SVs from 42 studies. See in: genome view    
Remapped(Score: Pass):1-65,496Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5941616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,083,98436,190,304
nsv5941616RemappedPassGRCh37.p13PATCHESFirst PassNW_003315949.1Chr17|NW_0
03315949.1
165,496

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17387698deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17387698Submitted genomicNC_000017.11:g.360
83984_36190304del
GRCh38 (hg38)NC_000017.11Chr1736,083,98436,190,304
nssv17387698RemappedPassNW_003315949.1:g.1
_65496del
GRCh37.p13First PassNW_003315949.1Chr17|NW_0
03315949.1
165,496

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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