A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3539718



Internal ID18740834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:51334744..51335310hg38UCSC Ensembl
Outerchr6:51334595..51335421hg38UCSC Ensembl
Innerchr6:51199542..51200108hg19UCSC Ensembl
Outerchr6:51199393..51200219hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9738465
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3539718
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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