A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637708



Internal ID6677809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4824434..4827162hg38UCSC Ensembl
Innerchr16:4824440..4827156hg38UCSC Ensembl
Outerchr16:4824428..4827168hg38UCSC Ensembl
chr16:4874435..4877163hg19UCSC Ensembl
Innerchr16:4874441..4877157hg19UCSC Ensembl
Outerchr16:4874429..4877169hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382729
hg192729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363818
SamplesNA12383
Known GenesGLYR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637708
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