A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032295



Internal ID18774829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80627422..80647440hg38UCSC Ensembl
Innerchr7:80256738..80276756hg19UCSC Ensembl
Innerchr7:80094674..80114692hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3820019
hg1920019
hg1820019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6515n100
Supporting Variantsnssv3655141, nssv3655142
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)nsv1032295
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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