A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv797463



Internal ID16091419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:60760228..60922010hg38UCSC Ensembl
Innerchr12:61154009..61315791hg19UCSC Ensembl
Innerchr12:59440276..59602058hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38161783
hg19161783
hg18161783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559147
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)nssv797463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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