A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798764



Internal ID18827288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162163721..162329060hg38UCSC Ensembl
Innerchr6:162584753..162750092hg19UCSC Ensembl
Innerchr6:162504743..162670082hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38165340
hg19165340
hg18165340
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=62
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798764
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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