A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017292



Internal ID21926635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138537921..138538306hg38UCSC Ensembl
chr5:137873610..137873995hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553359
Samples
Known GenesETF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017292
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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