A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557915



Internal ID15998638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29403406..29406294hg38UCSC Ensembl
Innerchr12:29556339..29559227hg19UCSC Ensembl
Innerchr12:29447606..29450494hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg382889
hg192889
hg182889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv790479
Samples
Known GenesOVCH1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557915
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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