A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551066



Internal ID21875421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68939445..68983746hg38UCSC Ensembl
chr5:68235272..68279573hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3844302
hg1944302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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