A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638303



Internal ID7025089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26776263..26778347hg38UCSC Ensembl
Innerchr16:26776263..26778347hg38UCSC Ensembl
Outerchr16:26776058..26778650hg38UCSC Ensembl
chr16:26787584..26789668hg19UCSC Ensembl
Innerchr16:26787584..26789668hg19UCSC Ensembl
Outerchr16:26787379..26789971hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382085
hg192085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15437247
SamplesHG00629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638303
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