A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3669672



Internal ID18621267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514849..143610780hg38UCSC Ensembl
Innerchr7:143211942..143307873hg19UCSC Ensembl
Innerchr7:142922064..143017995hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3895932
hg1995932
hg1895932
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026915
Supporting Variants
Samples
Known GenesCTAGE15, EPHA1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3669672
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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