A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033465



Internal ID18775998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143711325..143827101hg38UCSC Ensembl
Innerchr7:143408418..143524194hg19UCSC Ensembl
Innerchr7:143039351..143155127hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38115777
hg19115777
hg18115777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3670412
Samples
Known GenesCTAGE6, 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)nsv1033465
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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