A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603589



Internal ID16390998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:67265273..68155826hg38UCSC Ensembl
Innerchr6:67975166..68865718hg19UCSC Ensembl
Innerchr6:68031887..68922439hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38890554
hg19890553
hg18890553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1063565
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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