A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3669664



Internal ID18621259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143514550..143711325hg38UCSC Ensembl
Innerchr7:143211643..143408418hg19UCSC Ensembl
Innerchr7:142921765..143039351hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38196776
hg19196776
hg18117587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022170
Supporting Variants
Samples
Known GenesCTAGE15, 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)nssv3669664
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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