A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv791686



Internal ID15738956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31590385..31591155hg38UCSC Ensembl
Innerchr12:31743319..31744089hg19UCSC Ensembl
Innerchr12:31634586..31635356hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38771
hg19771
hg18771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558095
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)nssv791686
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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