A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020745



Internal ID18763279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80602341..80680179hg38UCSC Ensembl
Innerchr7:80231657..80309495hg19UCSC Ensembl
Innerchr7:80069593..80147431hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3877839
hg1977839
hg1877839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6514n100
Supporting Variantsnssv3755416
Samples
Known GenesCD36
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020745
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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