A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151047



Internal ID15875618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40606002..40663276hg38UCSC Ensembl
Innerchr2:40833142..40890416hg19UCSC Ensembl
Innerchr2:40686646..40743920hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3857275
hg1957275
hg1857275
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581508
Supporting Variants
SamplesHGDP00709
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151047
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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