A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155291



Internal ID15529960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12473176..12524502hg38UCSC Ensembl
Innerchr7:12512802..12564128hg19UCSC Ensembl
Innerchr7:12479327..12530653hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3851327
hg1951327
hg1851327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606228
Supporting Variants
SamplesHGDP00875
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155291
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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