A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779250



Internal ID19172283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80879772..80903648hg38UCSC Ensembl
Innerchr16:80913669..80937545hg19UCSC Ensembl
Innerchr16:79471170..79495046hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3823877
hg1923877
hg1823877
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892910
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779250
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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