A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019335



Internal ID21928678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172227676..172230953hg38UCSC Ensembl
chr5:171654680..171657957hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg383278
hg193278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568548
Samples
Known GenesUBTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019335
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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