A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528293



Internal ID15455586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88153203..88237319hg38UCSC Ensembl
InnerchrX:87408204..87492320hg19UCSC Ensembl
InnerchrX:87294860..87378976hg18UCSC Ensembl
InnerchrX:87214349..87298465hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3884117
hg1984117
hg1884117
hg1784117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704868
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528293
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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