A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608693



Internal ID16396102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143878890..144153772hg38UCSC Ensembl
Innerchr7:143575983..143850865hg19UCSC Ensembl
Innerchr7:143206916..143481798hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38274883
hg19274883
hg18274883
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11664n54
Supporting Variantsnssv1096542
Samples
Known GenesFAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608693
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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