A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600786



Internal ID16041509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:666450..667422hg38UCSC Ensembl
Innerchr6:666450..667422hg19UCSC Ensembl
Innerchr6:611450..612422hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38973
hg19973
hg18973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10267n54
Supporting Variantsnssv1047594, nssv1047595
Samples
Known GenesEXOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600786
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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