A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553030



Internal ID21877385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68142410..68174702hg38UCSC Ensembl
chr5:67438238..67470530hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3832293
hg1932293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553030
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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