A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929521



Internal ID20411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13577108..13677562hg38UCSC Ensembl
chr3:13618608..13719061hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38100455
hg19100454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447245
Supporting Variants
Samples
Known GenesFBLN2, LINC00620
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929521
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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