A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630347



Internal ID21822394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36583542..36583678hg38UCSC Ensembl
chr20:35211945..35212081hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042135
Supporting Variants
Samples
Known GenesTGIF2, TGIF2-C20orf24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630347
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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