A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15547115



Internal ID3901256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85012691..85023988hg38UCSC Ensembl
Innerchr16:85013191..85023488hg38UCSC Ensembl
Outerchr16:85011691..85024988hg38UCSC Ensembl
chr16:85046297..85057594hg19UCSC Ensembl
Innerchr16:85046797..85057094hg19UCSC Ensembl
Outerchr16:85045297..85058594hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3811298
hg1911298
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639450
Supporting Variants
SamplesHG03557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15547115
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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