A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058571



Internal ID15911757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:48837225..49027584hg38UCSC Ensembl
Innerchr6:48804862..48995221hg19UCSC Ensembl
Innerchr6:48912821..49103180hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38190360
hg19190360
hg18190360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603037
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058571
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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