A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739111



Internal ID18713357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119096353..119096634hg38UCSC Ensembl
Outerchr6:119096313..119096706hg38UCSC Ensembl
Innerchr6:119417518..119417799hg19UCSC Ensembl
Outerchr6:119417478..119417871hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540364
Supporting Variants
Samples
Known GenesFAM184A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739111
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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