A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16964270



Internal ID43487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35499274..35563000hg38UCSC Ensembl
chr5:35499376..35563102hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3863727
hg1963727
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16964270
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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