A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405160



Internal ID21062713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139579960..139586637hg38UCSC Ensembl
chr5:138959545..138966222hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg386678
hg196678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125981
Samples
Known GenesUBE2D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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