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nsv5508478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,103

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 36 studies. See in: genome view    
Submitted genomic50,375,232-50,390,334Question Mark
Overlapping variant regions from other studies: 162 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):50,769,015-50,784,117Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1250,375,23250,390,334
nsv5508478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1250,769,01550,784,117

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056483duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056483Submitted genomicNC_000012.12:g.503
75232_50390334dup
GRCh38 (hg38)NC_000012.12Chr1250,375,23250,390,334
nssv17056483RemappedPerfectNC_000012.11:g.507
69015_50784117dup
GRCh37.p13First PassNC_000012.11Chr1250,769,01550,784,117

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)
nssv170564830.00176404
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