A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070276



Internal ID20637316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63898687..63922983hg38UCSC Ensembl
chr20:62530040..62554336hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3824297
hg1924297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535791
Supporting Variants
Samples
Known GenesDNAJC5, MIR941-1, MIR941-2, MIR941-3, MIR941-4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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