A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155216



Internal ID15507612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80547768..80682478hg38UCSC Ensembl
Innerchr7:80177084..80311794hg19UCSC Ensembl
Innerchr7:80015020..80149730hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38134711
hg19134711
hg18134711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607682
Supporting Variants
Samples1780862075_A
Known GenesCD36
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155216
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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