A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608692



Internal ID16396101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143848626..144177097hg38UCSC Ensembl
Innerchr7:143545719..143874190hg19UCSC Ensembl
Innerchr7:143176652..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38328472
hg19328472
hg18328472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11664n54
Supporting Variantsnssv1156104, nssv1156103
SamplesHGDP00013, HGDP01293
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)nsv608692
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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