A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401089



Internal ID22458959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62145968..62146067hg38UCSC Ensembl
chr20:60721024..60721123hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960341
Supporting Variants
Samples
Known GenesSS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401089
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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