A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738806



Internal ID18712994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:81434717..81468765hg38UCSC Ensembl
Outerchr6:81434482..81469455hg38UCSC Ensembl
Innerchr6:82144434..82178482hg19UCSC Ensembl
Outerchr6:82144199..82179172hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3834974
hg1934974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738806
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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