A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783151



Internal ID18818559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41752698..41776423hg38UCSC Ensembl
Innerchr19:42256606..42280332hg19UCSC Ensembl
Innerchr19:46948446..46972172hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823726
hg1923727
hg1823727
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893209
Supporting Variants
Samples
Known GenesCEACAM6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783151
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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