A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523682



Internal ID15450975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88242756..88372009hg38UCSC Ensembl
InnerchrX:87497757..87627010hg19UCSC Ensembl
InnerchrX:87384413..87513666hg18UCSC Ensembl
InnerchrX:87303902..87433155hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38129254
hg19129254
hg18129254
hg17129254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv518n21
Supporting Variantsnssv699486
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523682
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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