A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3670388



Internal ID18968669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143549301..143816712hg38UCSC Ensembl
Innerchr7:143246394..143513805hg19UCSC Ensembl
Innerchr7:142956516..143144738hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38267412
hg19267412
hg18188223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024013
Supporting Variants
Samples
Known GenesCTAGE15, CTAGE6, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3670388
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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