A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604569



Internal ID16391978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:120473943..120566674hg38UCSC Ensembl
Innerchr6:120795089..120887820hg19UCSC Ensembl
Innerchr6:120836788..120929519hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3892732
hg1992732
hg1892732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072359
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604569
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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