A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528635



Internal ID15109242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:14087371..14467523hg38UCSC Ensembl
InnerchrX:14105490..14485645hg19UCSC Ensembl
InnerchrX:14015411..14395566hg18UCSC Ensembl
InnerchrX:13865147..14245302hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38380153
hg19380156
hg18380156
hg17380156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705265
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528635
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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