A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638257



Internal ID7025043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24674811..24683924hg38UCSC Ensembl
Innerchr16:24674816..24683919hg38UCSC Ensembl
Outerchr16:24674806..24683929hg38UCSC Ensembl
chr16:24686132..24695245hg19UCSC Ensembl
Innerchr16:24686137..24695240hg19UCSC Ensembl
Outerchr16:24686127..24695250hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg389114
hg199114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15431129
SamplesHG01699
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638257
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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