A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780612



Internal ID18834599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162165034..162318733hg38UCSC Ensembl
Innerchr6:162586066..162739765hg19UCSC Ensembl
Innerchr6:162506056..162659755hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38153700
hg19153700
hg18153700
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890980
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=60
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780612
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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