A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892808



Internal ID19183628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20535754..20554263hg38UCSC Ensembl
Outerchr16:20535562..20557521hg38UCSC Ensembl
Innerchr16:20547076..20565585hg19UCSC Ensembl
Outerchr16:20546884..20568843hg19UCSC Ensembl
Innerchr16:20454577..20473086hg18UCSC Ensembl
Outerchr16:20454385..20476344hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3821960
hg1921960
hg1821960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801424, essv25800513, essv25787381, essv25796112
Samples
Known GenesACSM2B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892808
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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