A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv796325



Internal ID15743595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:57517429..57522259hg38UCSC Ensembl
Innerchr12:57911212..57916042hg19UCSC Ensembl
Innerchr12:56197479..56202309hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg384831
hg194831
hg184831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559036
Supporting Variants
Samples
Known GenesDDIT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv796325
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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