A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539333



Internal ID20912631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44725812..44731370hg38UCSC Ensembl
chr20:43354453..43360011hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385559
hg195559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067850
Samples
Known GenesWISP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539333
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