A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801673



Internal ID15748943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:100738421..100809862hg38UCSC Ensembl
Innerchr12:101132199..101203640hg19UCSC Ensembl
Innerchr12:99656330..99727771hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3871442
hg1971442
hg1871442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560005
Supporting Variants
Samples
Known GenesANO4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801673
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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