A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567252



Internal ID18768328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9460158..9460479hg38UCSC Ensembl
Outerchr6:9460093..9460556hg38UCSC Ensembl
Innerchr6:9460391..9460712hg19UCSC Ensembl
Outerchr6:9460326..9460789hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765999
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567252
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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