A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551880



Internal ID21876235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138546875..138547009hg38UCSC Ensembl
chr5:137882564..137882698hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551880
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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