A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635620



Internal ID21827667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57848854..57848854hg38UCSC Ensembl
chr17:55926215..55926215hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086510
Supporting Variants
Samples
Known GenesMRPS23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635620
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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