A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069133



Internal ID20636173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58982400..58987692hg38UCSC Ensembl
chr20:57557455..57562747hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg385293
hg195293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552066
Supporting Variants
Samples
Known GenesNELFCD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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