A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2936n223



Internal ID22805904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75924898..76008798hg38UCSC Ensembl
chr16:75958796..76042696hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3883901
hg1983901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6506407, nsv6496907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2936n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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