A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892870



Internal ID19183690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63269405..63559278hg38UCSC Ensembl
Outerchr16:63269405..63559278hg38UCSC Ensembl
Innerchr16:63303309..63593182hg19UCSC Ensembl
Outerchr16:63303309..63593182hg19UCSC Ensembl
Innerchr16:61860810..62150683hg18UCSC Ensembl
Outerchr16:61860810..62150683hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38289874
hg19289874
hg18289874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799419
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892870
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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