A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796141



Internal ID18815256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1764390..1780436hg38UCSC Ensembl
Innerchr16:1814391..1830437hg19UCSC Ensembl
Innerchr16:1754392..1770438hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816047
hg1916047
hg1816047
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892756
Supporting Variants
Samples
Known GenesEME2, MAPK8IP3, MRPS34, NME3, SPSB3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796141
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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