A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787395



Internal ID19175880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162038539..162099101hg38UCSC Ensembl
Innerchr6:162459571..162520133hg19UCSC Ensembl
Innerchr6:162379561..162440123hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3860563
hg1960563
hg1860563
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890979
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787395
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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