A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533765



Internal ID20907126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21972979..22180646hg38UCSC Ensembl
chr19:22155781..22363448hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38207668
hg19207668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047359
Samples
Known GenesZNF208, ZNF257, ZNF676
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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