A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541959



Internal ID21866314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61282627..61282712hg38UCSC Ensembl
chr5:60578454..60578539hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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