A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16972704



Internal ID49167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116905822..116905921hg38UCSC Ensembl
chr5:116241518..116241617hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461348
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16972704
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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