A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv800818



Internal ID16094774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95617401..95618311hg38UCSC Ensembl
Innerchr12:96011177..96012087hg19UCSC Ensembl
Innerchr12:94535308..94536218hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559826
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)nssv800818
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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