A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892854



Internal ID19183674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35962309..36034953hg38UCSC Ensembl
Outerchr16:35934461..36050028hg38UCSC Ensembl
Innerchr16:35196680..35269324hg19UCSC Ensembl
Outerchr16:35168832..35284399hg19UCSC Ensembl
Innerchr16:35054181..35126825hg18UCSC Ensembl
Outerchr16:35026333..35141900hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38115568
hg19115568
hg18115568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786549, essv25799876, essv25787231
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892854
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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