A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788036



Internal ID18834327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162239956..162629816hg38UCSC Ensembl
Innerchr6:162660988..163050848hg19UCSC Ensembl
Innerchr6:162580978..162970838hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38389861
hg19389861
hg18389861
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890984
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=107
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788036
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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