A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701029



Internal ID15437681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95059392..95120990hg38UCSC Ensembl
InnerchrX:94314391..94375989hg19UCSC Ensembl
InnerchrX:94201047..94262645hg18UCSC Ensembl
InnerchrX:94120536..94182134hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3861599
hg1961599
hg1861599
hg1761599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524998
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701029
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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