A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv797691



Internal ID16091647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:69895940..69896854hg38UCSC Ensembl
Innerchr12:70289720..70290634hg19UCSC Ensembl
Innerchr12:68575987..68576901hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38915
hg19915
hg18915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559228
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)nssv797691
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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