A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538799



Internal ID21863154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8259904..8260597hg38UCSC Ensembl
chr5:8260017..8260710hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538799
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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