A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739547



Internal ID18367107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162162824..162165408hg38UCSC Ensembl
Outerchr6:162162697..162165909hg38UCSC Ensembl
Innerchr6:162583856..162586440hg19UCSC Ensembl
Outerchr6:162583729..162586941hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383213
hg193213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540800
Supporting Variants
Samples
Known GenesPARK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739547
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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