A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540769



Internal ID18395159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:159934676..159934813hg38UCSC Ensembl
Outerchr6:159934669..159934820hg38UCSC Ensembl
Innerchr6:160355708..160355845hg19UCSC Ensembl
Outerchr6:160355701..160355852hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739516
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540769
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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