A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639450



Internal ID7026231
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15547111, essv15547114, essv15547115, essv15547112, essv15547113
SamplesHG02562, HG03460, HG03363, HG03557, HG01914
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639450
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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