A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560152



Internal ID21884507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145728961..145746873hg38UCSC Ensembl
chr5:145108524..145126436hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3817913
hg1917913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560152
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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