A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154876



Internal ID15855270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:118446987..118540100hg38UCSC Ensembl
Innerchr6:118768150..118861263hg19UCSC Ensembl
Innerchr6:118874843..118967956hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3893114
hg1993114
hg1893114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604558
Supporting Variants
Samples1780862529_A
Known GenesBRD7P3, CEP85L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154876
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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