A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv791665



Internal ID15738935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31589529..31590945hg38UCSC Ensembl
Innerchr12:31742463..31743879hg19UCSC Ensembl
Innerchr12:31633730..31635146hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381417
hg191417
hg181417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558088
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)nssv791665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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