A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638259



Internal ID7025045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24831962..24833063hg38UCSC Ensembl
Innerchr16:24832012..24833013hg38UCSC Ensembl
Outerchr16:24831821..24833204hg38UCSC Ensembl
chr16:24843283..24844384hg19UCSC Ensembl
Innerchr16:24843333..24844334hg19UCSC Ensembl
Outerchr16:24843142..24844525hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15431132, essv15431133
SamplesHG02271, HG01979
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638259
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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