A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528197



Internal ID15455490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69103917..69122733hg38UCSC Ensembl
InnerchrX:68323760..68342576hg19UCSC Ensembl
InnerchrX:68240485..68259301hg18UCSC Ensembl
InnerchrX:68106781..68125597hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3818817
hg1918817
hg1818817
hg1718817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704756
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528197
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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