A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605020



Internal ID16392429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160843572..160857737hg38UCSC Ensembl
Innerchr6:161264604..161278769hg19UCSC Ensembl
Innerchr6:161184594..161198759hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3814166
hg1914166
hg1814166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10991n54
Supporting Variantsnssv1075204
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605020
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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