A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782960



Internal ID18827257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161452979..161535643hg38UCSC Ensembl
Innerchr6:161874011..161956675hg19UCSC Ensembl
Innerchr6:161794001..161876665hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3882665
hg1982665
hg1882665
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890978
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=45
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782960
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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