A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068154



Internal ID20635194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51898881..51920567hg38UCSC Ensembl
chr20:50515420..50537106hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3821687
hg1921687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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