A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739098



Internal ID18713344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:116429712..116429964hg38UCSC Ensembl
Outerchr6:116429648..116430001hg38UCSC Ensembl
Innerchr6:116750875..116751127hg19UCSC Ensembl
Outerchr6:116750811..116751164hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540351
Supporting Variants
Samples
Known GenesDSE
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739098
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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