A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524646



Internal ID15451939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98512955..98702073hg38UCSC Ensembl
InnerchrX:97767953..97957071hg19UCSC Ensembl
InnerchrX:97654609..97843727hg18UCSC Ensembl
InnerchrX:97574098..97763216hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38189119
hg19189119
hg18189119
hg17189119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700612
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524646
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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