A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150396



Internal ID15877947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062091..13142111hg38UCSC Ensembl
Innerchr2:13202216..13282236hg19UCSC Ensembl
Innerchr2:13119667..13199687hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3880021
hg1980021
hg1880021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581010
Supporting Variants
SamplesHGDP01072
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150396
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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