A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600066



Internal ID21792113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75169194..75169261hg38UCSC Ensembl
chr15:75461535..75461602hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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