A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634950



Internal ID21826997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62148267..62148361hg38UCSC Ensembl
chr20:60723323..60723417hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040584
Supporting Variants
Samples
Known GenesSS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634950
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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