A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639410



Internal ID6679503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84055831..84075312hg38UCSC Ensembl
Innerchr16:84055848..84075296hg38UCSC Ensembl
Outerchr16:84055815..84075329hg38UCSC Ensembl
chr16:84089436..84108917hg19UCSC Ensembl
Innerchr16:84089453..84108901hg19UCSC Ensembl
Outerchr16:84089420..84108934hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3819482
hg1919482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15545793, essv15545794
SamplesHG00182, HG03920
Known GenesMBTPS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639410
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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