A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724337



Internal ID148003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57435161..57435254hg38UCSC Ensembl
chr19:57946529..57946622hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724337
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.030998


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