A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639536



Internal ID6679628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87934495..87946252hg38UCSC Ensembl
Innerchr16:87934495..87946252hg38UCSC Ensembl
Outerchr16:87934385..87946342hg38UCSC Ensembl
chr16:87968101..87979858hg19UCSC Ensembl
Innerchr16:87968101..87979858hg19UCSC Ensembl
Outerchr16:87967991..87979948hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3811758
hg1911758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15556041
SamplesNA12286
Known GenesCA5A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639536
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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