A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964227



Internal ID43456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34838198..34838291hg38UCSC Ensembl
chr5:34838303..34838396hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964227
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001561


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