A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892877



Internal ID19183697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65816030..65847477hg38UCSC Ensembl
Outerchr16:65816030..65847477hg38UCSC Ensembl
Innerchr16:65849933..65881380hg19UCSC Ensembl
Outerchr16:65849933..65881380hg19UCSC Ensembl
Innerchr16:64407434..64438881hg18UCSC Ensembl
Outerchr16:64407434..64438881hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3831448
hg1931448
hg1831448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789853
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892877
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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