A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639491



Internal ID7026271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86795992..86829634hg38UCSC Ensembl
Innerchr16:86796008..86829618hg38UCSC Ensembl
Outerchr16:86795976..86829650hg38UCSC Ensembl
chr16:86829598..86863240hg19UCSC Ensembl
Innerchr16:86829614..86863224hg19UCSC Ensembl
Outerchr16:86829582..86863256hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3833643
hg1933643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15553964, essv15553965
SamplesNA19900, HG03072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639491
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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