A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016229



Internal ID21925572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139617450..139617510hg38UCSC Ensembl
chr5:138997035..138997095hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554484
Samples
Known GenesUBE2D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016229
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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