A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637672



Internal ID7024462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3634312..3643832hg38UCSC Ensembl
Innerchr16:3634347..3643798hg38UCSC Ensembl
Outerchr16:3634278..3643867hg38UCSC Ensembl
chr16:3684313..3693833hg19UCSC Ensembl
Innerchr16:3684348..3693799hg19UCSC Ensembl
Outerchr16:3684279..3693868hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389521
hg199521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363261
SamplesNA20787
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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