A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545788



Internal ID20919014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50170601..50173000hg38UCSC Ensembl
chr20:48787138..48789537hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545788
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