A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543591



Internal ID21867946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113619056..113629670hg38UCSC Ensembl
chr5:112954753..112965367hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3810615
hg1910615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543591
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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