A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893209



Internal ID19184029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41755151..41767097hg38UCSC Ensembl
Outerchr19:41752698..41776423hg38UCSC Ensembl
Innerchr19:42259059..42271006hg19UCSC Ensembl
Outerchr19:42256606..42280332hg19UCSC Ensembl
Innerchr19:46950899..46962846hg18UCSC Ensembl
Outerchr19:46948446..46972172hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823726
hg1923727
hg1823727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783151, essv25783108, essv25797677, essv25800534
Samples
Known GenesCEACAM6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893209
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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