A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797730



Internal ID18825307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162232577..162288915hg38UCSC Ensembl
Innerchr6:162653609..162709947hg19UCSC Ensembl
Innerchr6:162573599..162629937hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3856339
hg1956339
hg1856339
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890981
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797730
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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