A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797677



Internal ID18826085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41755151..41767097hg38UCSC Ensembl
Innerchr19:42259059..42271006hg19UCSC Ensembl
Innerchr19:46950899..46962846hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3811947
hg1911948
hg1811948
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 Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797677
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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