A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15489799



Internal ID660748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58933846..58941373hg38UCSC Ensembl
Innerchr16:58933846..58941373hg38UCSC Ensembl
Outerchr16:58933572..58941597hg38UCSC Ensembl
chr16:58967750..58975277hg19UCSC Ensembl
Innerchr16:58967750..58975277hg19UCSC Ensembl
Outerchr16:58967476..58975501hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387528
hg197528
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638735
Supporting Variants
SamplesHG00306
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15489799
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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