A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567732



Internal ID18768808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44645762..44646066hg38UCSC Ensembl
Outerchr6:44645712..44646130hg38UCSC Ensembl
Innerchr6:44613499..44613803hg19UCSC Ensembl
Outerchr6:44613449..44613867hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv387e215
Supporting Variantsessv9766479
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567732
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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