A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892918



Internal ID18837052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82931460..83009567hg38UCSC Ensembl
Outerchr16:82916897..83009568hg38UCSC Ensembl
Innerchr16:82965065..83043172hg19UCSC Ensembl
Outerchr16:82950502..83043173hg19UCSC Ensembl
Innerchr16:81522566..81600673hg18UCSC Ensembl
Outerchr16:81508003..81600674hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3892672
hg1992672
hg1892672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797230, essv25796361, essv25779831, essv25796986, essv25801095
Samples
Known GenesCDH13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892918
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer