A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565238



Internal ID21889593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169051416..169051416hg38UCSC Ensembl
chr5:168478421..168478421hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067024
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565238
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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