A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016718



Internal ID19105935
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 StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3669692
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)nsv1016718
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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