A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559367



Internal ID16346776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:72737035..72991316hg38UCSC Ensembl
Innerchr12:73130815..73385096hg19UCSC Ensembl
Innerchr12:71417082..71671363hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38254282
hg19254282
hg18254282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv798609
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559367
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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