A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543129



Internal ID21867484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140635080..140638808hg38UCSC Ensembl
chr5:140014665..140018393hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg383729
hg193729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543129
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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