A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600783



Internal ID16041506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:601400..602414hg38UCSC Ensembl
Innerchr6:601400..602414hg19UCSC Ensembl
Innerchr6:546400..547414hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381015
hg191015
hg181015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1047591
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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