A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892934



Internal ID18837068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87743983..87755230hg38UCSC Ensembl
Outerchr16:87743983..87755230hg38UCSC Ensembl
Innerchr16:87777589..87788836hg19UCSC Ensembl
Outerchr16:87777589..87788836hg19UCSC Ensembl
Innerchr16:86335090..86346337hg18UCSC Ensembl
Outerchr16:86335090..86346337hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3811248
hg1911248
hg1811248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779167
Samples
Known GenesKLHDC4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892934
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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