A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067180



Internal ID20634220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25643557..25651034hg38UCSC Ensembl
chr20:25624193..25631670hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg387478
hg197478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533634
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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