A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv791669



Internal ID15738939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31590260..31590891hg38UCSC Ensembl
Innerchr12:31743194..31743825hg19UCSC Ensembl
Innerchr12:31634461..31635092hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38632
hg19632
hg18632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558090
Supporting Variants
Samples
Known GenesDENND5B, DENND5B-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv791669
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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