A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608682



Internal ID16049405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143444382..144177097hg38UCSC Ensembl
Innerchr7:143141475..143874190hg19UCSC Ensembl
Innerchr7:142851597..143505123hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38732716
hg19732716
hg18653527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1096531
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, FAM115C, LOC154761, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, OR2F1, OR2F2, OR6B1, TAS2R41, TAS2R60
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608682
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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