A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655139



Internal ID18606734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80626939..80643409hg38UCSC Ensembl
Innerchr7:80256255..80272725hg19UCSC Ensembl
Innerchr7:80094191..80110661hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3816471
hg1916471
hg1816471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023254
Supporting Variants
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)nssv3655139
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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