A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601056



Internal ID16388465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18714952..19116208hg38UCSC Ensembl
Innerchr6:18715183..19116439hg19UCSC Ensembl
Innerchr6:18823162..19224418hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38401257
hg19401257
hg18401257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10311n54
Supporting Variantsnssv1050623
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601056
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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