A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695480



Internal ID15432132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:84510546..84527906hg38UCSC Ensembl
InnerchrX:83765554..83782914hg19UCSC Ensembl
InnerchrX:83652210..83669570hg18UCSC Ensembl
InnerchrX:83571699..83589059hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3817361
hg1917361
hg1817361
hg1717361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520647
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695480
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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