A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008207



Internal ID21917550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159171637..159172183hg38UCSC Ensembl
chr5:158598645..158599191hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565005
Samples
Known GenesRNF145
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008207
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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