A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639340



Internal ID7026122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81718109..81720240hg38UCSC Ensembl
Innerchr16:81718128..81720222hg38UCSC Ensembl
Outerchr16:81718091..81720259hg38UCSC Ensembl
chr16:81751714..81753845hg19UCSC Ensembl
Innerchr16:81751733..81753827hg19UCSC Ensembl
Outerchr16:81751696..81753864hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg382132
hg192132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15537870
SamplesHG01847
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639340
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