A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600784



Internal ID16041507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:658461..667756hg38UCSC Ensembl
Innerchr6:658461..667756hg19UCSC Ensembl
Innerchr6:603461..612756hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg389296
hg199296
hg189296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1047592
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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