A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053070



Internal ID15906256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31316567..31350367hg38UCSC Ensembl
Innerchr6:31284344..31318144hg19UCSC Ensembl
Innerchr6:31392323..31426123hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3833801
hg1933801
hg1833801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601700
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)nssv1053070
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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