A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892880



Internal ID18837014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70123665..70157430hg38UCSC Ensembl
Outerchr16:70107584..70162409hg38UCSC Ensembl
Innerchr16:70157568..70191333hg19UCSC Ensembl
Outerchr16:70141487..70196312hg19UCSC Ensembl
Innerchr16:68715069..68748834hg18UCSC Ensembl
Outerchr16:68698988..68753813hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3854826
hg1954826
hg1854826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786699, essv25786204
Samples
Known GenesPDPR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892880
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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