A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525891



Internal ID20899252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4950651..4991329hg38UCSC Ensembl
chr20:4931297..4971975hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3840679
hg1940679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068998
Samples
Known GenesSLC23A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525891
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