A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525862



Internal ID15453155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:79872691..79942877hg38UCSC Ensembl
InnerchrX:79128191..79198373hg19UCSC Ensembl
InnerchrX:79014847..79085029hg18UCSC Ensembl
InnerchrX:78934336..79004518hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3870187
hg1970183
hg1870183
hg1770183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702058
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525862
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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