A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363258



Internal ID5365074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3612113..3634450hg38UCSC Ensembl
Innerchr16:3612613..3633950hg38UCSC Ensembl
Outerchr16:3611113..3635450hg38UCSC Ensembl
chr16:3662114..3684451hg19UCSC Ensembl
Innerchr16:3662614..3683951hg19UCSC Ensembl
Outerchr16:3661114..3685451hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3822338
hg1922338
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637670
Supporting Variants
SamplesHG01389
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363258
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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