A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070272



Internal ID20637312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63841701..63850400hg38UCSC Ensembl
chr20:62473054..62481753hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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