A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892922



Internal ID18837056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83308629..83315793hg38UCSC Ensembl
Outerchr16:83308629..83315793hg38UCSC Ensembl
Innerchr16:83342234..83349398hg19UCSC Ensembl
Outerchr16:83342234..83349398hg19UCSC Ensembl
Innerchr16:81899735..81906899hg18UCSC Ensembl
Outerchr16:81899735..81906899hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg387165
hg197165
hg187165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782704
Samples
Known GenesCDH13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892922
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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