A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526778



Internal ID15107385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9138192..9163530hg38UCSC Ensembl
Innerchr11:9159739..9185077hg19UCSC Ensembl
Innerchr11:9116315..9141653hg18UCSC Ensembl
Innerchr11:9116315..9141653hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825339
hg1925339
hg1825339
hg1725339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703130
Samples
Known GenesDENND5A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526778
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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