A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561726



Internal ID21886081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173334298..173336115hg38UCSC Ensembl
chr5:172761301..172763118hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg381818
hg191818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561726
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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