A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383845



Internal ID21041398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21027696..21594616hg38UCSC Ensembl
chr5:21027805..21594725hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38566921
hg19566921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215653
Samples
Known GenesGUSBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383845
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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