A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892933



Internal ID19183753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86700641..86724933hg38UCSC Ensembl
Outerchr16:86700641..86724933hg38UCSC Ensembl
Innerchr16:86734247..86758539hg19UCSC Ensembl
Outerchr16:86734247..86758539hg19UCSC Ensembl
Innerchr16:85291748..85316040hg18UCSC Ensembl
Outerchr16:85291748..85316040hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3824293
hg1924293
hg1824293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800723
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892933
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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