A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798861



Internal ID16092817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:74464177..74537569hg38UCSC Ensembl
Innerchr12:74857957..74931349hg19UCSC Ensembl
Innerchr12:73144224..73217616hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3873393
hg1973393
hg1873393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559417
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)nssv798861
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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