A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv796744



Internal ID16090700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:60125061..60146327hg38UCSC Ensembl
Innerchr12:60518842..60540108hg19UCSC Ensembl
Innerchr12:58805109..58826375hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3821267
hg1921267
hg1821267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559107
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)nssv796744
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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