A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638708



Internal ID6678805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57011492..57014264hg38UCSC Ensembl
Innerchr16:57011519..57014238hg38UCSC Ensembl
Outerchr16:57011466..57014291hg38UCSC Ensembl
chr16:57045404..57048176hg19UCSC Ensembl
Innerchr16:57045431..57048150hg19UCSC Ensembl
Outerchr16:57045378..57048203hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg382773
hg192773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15483342
SamplesNA19901
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638708
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer