A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15551798



Internal ID5553614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85192805..85201062hg38UCSC Ensembl
Innerchr16:85192805..85201062hg38UCSC Ensembl
Outerchr16:85192528..85201356hg38UCSC Ensembl
chr16:85226411..85234668hg19UCSC Ensembl
Innerchr16:85226411..85234668hg19UCSC Ensembl
Outerchr16:85226134..85234962hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg388258
hg198258
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639458
Supporting Variants
SamplesHG00309
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15551798
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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