A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798833



Internal ID16092789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:74135050..74216080hg38UCSC Ensembl
Innerchr12:74528830..74609860hg19UCSC Ensembl
Innerchr12:72815097..72896127hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3881031
hg1981031
hg1881031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559394
Supporting Variants
Samples
Known GenesLOC100507377
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv798833
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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