A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156105



Internal ID15880070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143878890..144177097hg38UCSC Ensembl
Innerchr7:143575983..143874190hg19UCSC Ensembl
Innerchr7:143206916..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38298208
hg19298208
hg18298208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608694
Supporting Variants
SamplesNINDS_149
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)nssv1156105
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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