A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066625



Internal ID20633665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16947552..16948526hg38UCSC Ensembl
chr20:16928197..16929171hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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