A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15547061



Internal ID2288390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84678120..84684031hg38UCSC Ensembl
Innerchr16:84678120..84684031hg38UCSC Ensembl
Outerchr16:84677620..84684531hg38UCSC Ensembl
chr16:84711726..84717637hg19UCSC Ensembl
Innerchr16:84711726..84717637hg19UCSC Ensembl
Outerchr16:84711226..84718137hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg385912
hg195912
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639441
Supporting Variants
SamplesHG02048
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15547061
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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