A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655637



Internal ID18953918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68745462..69082379hg38UCSC Ensembl
Innerchr7:68210449..68547366hg19UCSC Ensembl
Innerchr7:67848385..68185302hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38336918
hg19336918
hg18336918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023766
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655637
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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