A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892757



Internal ID19183577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2649303..2693417hg38UCSC Ensembl
Outerchr16:2617854..2693417hg38UCSC Ensembl
Innerchr16:2699304..2743418hg19UCSC Ensembl
Outerchr16:2667855..2743418hg19UCSC Ensembl
Innerchr16:2639305..2683419hg18UCSC Ensembl
Outerchr16:2607856..2683419hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3875564
hg1975564
hg1875564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788037, essv25788859
Samples
Known GenesERVK13-1, FLJ42627, KCTD5, LOC652276
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892757
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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