A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608756



Internal ID16396165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144210030..144377206hg38UCSC Ensembl
Innerchr7:143907123..144074299hg19UCSC Ensembl
Innerchr7:143538056..143705232hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38167177
hg19167177
hg18167177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11668n54
Supporting Variantsnssv1096638
Samples
Known GenesARHGEF34P, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608756
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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