A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019958



Internal ID21929301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158993068..158993190hg38UCSC Ensembl
chr5:158420076..158420198hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563388
Samples
Known GenesEBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019958
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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