A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685432



Internal ID15422084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113954140..113967564hg38UCSC Ensembl
InnerchrX:113197425..113210824hg19UCSC Ensembl
InnerchrX:113083690..113097089hg18UCSC Ensembl
InnerchrX:113003179..113016578hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3813425
hg1913400
hg1813400
hg1713400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685432
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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