A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569962



Internal ID21762005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152623239..152623296hg38UCSC Ensembl
chr5:152002799..152002856hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569962
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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