A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363261



Internal ID6624269
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637672
Supporting Variants
SamplesNA20787
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363261
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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