A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639506



Internal ID7026286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87270753..87285967hg38UCSC Ensembl
Innerchr16:87270903..87285817hg38UCSC Ensembl
Outerchr16:87270603..87286117hg38UCSC Ensembl
chr16:87304359..87319573hg19UCSC Ensembl
Innerchr16:87304509..87319423hg19UCSC Ensembl
Outerchr16:87304209..87319723hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3815215
hg1915215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15555121
SamplesHG01805
Known GenesLOC101928682
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639506
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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