A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525059



Internal ID20898420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23129321..23131423hg38UCSC Ensembl
chr20:23109958..23112060hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382103
hg192103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066840
Samples
Known GenesLINC00656
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525059
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