A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779167



Internal ID18817660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87743983..87755230hg38UCSC Ensembl
Innerchr16:87777589..87788836hg19UCSC Ensembl
Innerchr16:86335090..86346337hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3811248
hg1911248
hg1811248
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892934
Supporting Variants
Samples
Known GenesKLHDC4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779167
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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