A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798615



Internal ID16092571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73173597..73207706hg38UCSC Ensembl
Innerchr12:73567377..73601486hg19UCSC Ensembl
Innerchr12:71853644..71887753hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3834110
hg1934110
hg1834110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559372
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv798615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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