A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551631



Internal ID20924762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53454261..53458829hg38UCSC Ensembl
chr20:52070800..52075368hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384569
hg194569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067864
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551631
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