A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784804



Internal ID18824540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8628195..8656246hg38UCSC Ensembl
Innerchr16:8722052..8750103hg19UCSC Ensembl
Innerchr16:8629553..8657604hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3828052
hg1928052
hg1828052
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892786
Supporting Variants
Samples
Known GenesMETTL22
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784804
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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