A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067850



Internal ID20634890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44725812..44731370hg38UCSC Ensembl
chr20:43354453..43360011hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385559
hg195559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539333
Supporting Variants
Samples
Known GenesWISP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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