A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3669692



Internal ID18967973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514849..143790559hg38UCSC Ensembl
Innerchr7:143211942..143487652hg19UCSC Ensembl
Innerchr7:142922064..143118585hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38275711
hg19275711
hg18196522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016718
Supporting Variants
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3669692
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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