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nsv5945032

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 133 SVs from 25 studies. See in: genome view    
Submitted genomic38,630,224-38,630,274Question Mark
Overlapping variant regions from other studies: 133 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):39,120,864-39,120,914Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5945032Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1938,630,22438,630,274
nsv5945032RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1939,120,86439,120,914

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17401598deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17401598Submitted genomicNC_000019.10:g.386
30224_38630274del
GRCh38 (hg38)NC_000019.10Chr1938,630,22438,630,274
nssv17401598RemappedPerfectNC_000019.9:g.3912
0864_39120914del
GRCh37.p13First PassNC_000019.9Chr1939,120,86439,120,914

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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