A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv797588



Internal ID16091544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:68858935..68862663hg38UCSC Ensembl
Innerchr12:69252715..69256443hg19UCSC Ensembl
Innerchr12:67538982..67542710hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg383729
hg193729
hg183729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559220
Supporting Variants
Samples
Known GenesCPM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv797588
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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