A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526259



Internal ID15453552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98582884..98683088hg38UCSC Ensembl
InnerchrX:97837882..97938086hg19UCSC Ensembl
InnerchrX:97724538..97824742hg18UCSC Ensembl
InnerchrX:97644027..97744231hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38100205
hg19100205
hg18100205
hg17100205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv521n21
Supporting Variantsnssv702531
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526259
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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