A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000160



Internal ID21909503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:50333629..50418927hg38UCSC Ensembl
chr5:49629463..49714761hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3885299
hg1985299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550685
Samples
Known GenesEMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000160
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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