A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890039



Internal ID167492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145301587..145574587hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38273001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890039
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000314


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