A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528648



Internal ID15455941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42102899..42120885hg38UCSC Ensembl
Innerchr11:42124449..42142435hg19UCSC Ensembl
Innerchr11:42081025..42099011hg18UCSC Ensembl
Innerchr11:42081025..42099011hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3817987
hg1917987
hg1817987
hg1717987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705281
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528648
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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