A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704597



Internal ID15441249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:74329492..74349044hg38UCSC Ensembl
InnerchrX:73549327..73568879hg19UCSC Ensembl
InnerchrX:73466052..73485604hg18UCSC Ensembl
InnerchrX:73332348..73351900hg17UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3819553
hg1919553
hg1819553
hg1719553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520605
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704597
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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