A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026688



Internal ID18769219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80602341..80677920hg38UCSC Ensembl
Innerchr7:80231657..80307236hg19UCSC Ensembl
Innerchr7:80069593..80145172hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3875580
hg1975580
hg1875580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6514n100
Supporting Variantsnssv3755415, nssv3755414
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)nsv1026688
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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