A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723005



Internal ID146671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35297966..35298105hg38UCSC Ensembl
chr19:35788869..35789008hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516706
Supporting Variants
Samples
Known GenesMAG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723005
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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