A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051648



Internal ID15904834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27490234..27580013hg38UCSC Ensembl
Innerchr6:27458013..27547792hg19UCSC Ensembl
Innerchr6:27565992..27655771hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3889780
hg1989780
hg1889780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601203
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)nssv1051648
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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