A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176267



Internal ID15532203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31113353..31255577hg38UCSC Ensembl
Innerchr12:31266287..31408511hg19UCSC Ensembl
Innerchr12:31157554..31299778hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38142225
hg19142225
hg18142225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558044
Supporting Variants
SamplesHGDP01274
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176267
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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