A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892756



Internal ID18836890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1764390..1780436hg38UCSC Ensembl
Outerchr16:1764390..1780436hg38UCSC Ensembl
Innerchr16:1814391..1830437hg19UCSC Ensembl
Outerchr16:1814391..1830437hg19UCSC Ensembl
Innerchr16:1754392..1770438hg18UCSC Ensembl
Outerchr16:1754392..1770438hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816047
hg1916047
hg1816047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796141
Samples
Known GenesEME2, MAPK8IP3, MRPS34, NME3, SPSB3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892756
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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