A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779975



Internal ID19169844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65363379..65688177hg38UCSC Ensembl
Innerchr16:65397282..65722080hg19UCSC Ensembl
Innerchr16:63954783..64279581hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38324799
hg19324799
hg18324799
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892876
Supporting Variants
Samples
Known GenesLINC00922
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=81
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779975
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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