A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604566



Internal ID16391975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120103739..120188045hg38UCSC Ensembl
Innerchr6:120424885..120509191hg19UCSC Ensembl
Innerchr6:120466584..120550890hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3884307
hg1984307
hg1884307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072356
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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