A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892917



Internal ID18837051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82679946..82693813hg38UCSC Ensembl
Outerchr16:82679946..82693813hg38UCSC Ensembl
Innerchr16:82713551..82727418hg19UCSC Ensembl
Outerchr16:82713551..82727418hg19UCSC Ensembl
Innerchr16:81271052..81284919hg18UCSC Ensembl
Outerchr16:81271052..81284919hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3813868
hg1913868
hg1813868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799236
Samples
Known GenesCDH13, MIR8058
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892917
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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