A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3539953



Internal ID18741029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71832811..71832954hg38UCSC Ensembl
Outerchr6:71832803..71832965hg38UCSC Ensembl
Innerchr6:72542514..72542657hg19UCSC Ensembl
Outerchr6:72542506..72542668hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9738700
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3539953
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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