A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540201



Internal ID21864556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:59897288..59901636hg38UCSC Ensembl
chr4:60763006..60767354hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg384349
hg194349
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540201
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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