A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268113



Internal ID20477331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59909225..59909280hg38UCSC Ensembl
chr17:57986586..57986641hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737321
Supporting Variants
Samples
Known GenesRPS6KB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268113
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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