A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739519



Internal ID18713765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160580951..160582959hg38UCSC Ensembl
Outerchr6:160580918..160583256hg38UCSC Ensembl
Innerchr6:161001983..161003991hg19UCSC Ensembl
Outerchr6:161001950..161004288hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382339
hg192339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540772
Supporting Variants
Samples
Known GenesLPA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739519
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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