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nsv5493106

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 267 SVs from 53 studies. See in: genome view    
Submitted genomic50,086,368-50,112,368Question Mark
Overlapping variant regions from other studies: 45 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):265,543-291,543Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5493106Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1050,086,36850,112,368
nsv5493106RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004504302.1Chr10|NW_0
04504302.1
265,543291,543

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17034662duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17034662Submitted genomicNC_000010.11:g.500
86368_50112368dup
GRCh38 (hg38)NC_000010.11Chr1050,086,36850,112,368
nssv17034662RemappedPerfectNW_004504302.1:g.2
65543_291543dup
GRCh37.p13First PassNW_004504302.1Chr10|NW_0
04504302.1
265,543291,543

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)
nssv17034662<0.00116402
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