A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069152



Internal ID20636192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59493073..59495178hg38UCSC Ensembl
chr20:58068128..58070233hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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