A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792146



Internal ID18817601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161381113..161650603hg38UCSC Ensembl
Innerchr6:161802145..162071635hg19UCSC Ensembl
Innerchr6:161722135..161991625hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38269491
hg19269491
hg18269491
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890977
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=130
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792146
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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