A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203453



Internal ID20770493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64288701..64292400hg38UCSC Ensembl
chr20:62920054..62923753hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552930
Supporting Variants
Samples
Known GenesLINC00266-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203453
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00037


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer