A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521301



Internal ID15101908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15412004..15429936hg38UCSC Ensembl
InnerchrX:15430126..15448059hg19UCSC Ensembl
InnerchrX:15340047..15357980hg18UCSC Ensembl
InnerchrX:15189783..15207716hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3817933
hg1917934
hg1817934
hg1717934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694431
Samples
Known GenesPIR, PIR-FIGF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521301
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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