A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799865



Internal ID18813261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162221692..162282387hg38UCSC Ensembl
Innerchr6:162642724..162703419hg19UCSC Ensembl
Innerchr6:162562714..162623409hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3860696
hg1960696
hg1860696
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 HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799865
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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