A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553176



Internal ID20926285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43463009..43463120hg38UCSC Ensembl
chr20:42091649..42091760hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067767
Samples
Known GenesSRSF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553176
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