A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540922



Internal ID21865277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38867917..38867994hg38UCSC Ensembl
chr5:38868019..38868096hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999672
Supporting Variants
Samples
Known GenesOSMR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540922
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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