A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798822



Internal ID16092778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73711122..73719248hg38UCSC Ensembl
Innerchr12:74104902..74113028hg19UCSC Ensembl
Innerchr12:72391169..72399295hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg388127
hg198127
hg188127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559384
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)nssv798822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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