A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637812



Internal ID7024600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7863345..7928453hg38UCSC Ensembl
Innerchr16:7863345..7928453hg38UCSC Ensembl
Outerchr16:7862845..7928953hg38UCSC Ensembl
chr16:7913347..7978455hg19UCSC Ensembl
Innerchr16:7913347..7978455hg19UCSC Ensembl
Outerchr16:7912847..7978955hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3865109
hg1965109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15368117
SamplesNA06994
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637812
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