A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799008



Internal ID19166877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4789025..4823964hg38UCSC Ensembl
Innerchr6:4789259..4824198hg19UCSC Ensembl
Innerchr6:4734258..4769197hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3834940
hg1934940
hg1834940
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890784
Supporting Variants
Samples
Known GenesCDYL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799008
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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