A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974214



Internal ID50182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:127915433..127928817hg38UCSC Ensembl
chr5:127251125..127264509hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3813385
hg1913385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5464529
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974214
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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