A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608938



Internal ID21800985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89765617..89765752hg38UCSC Ensembl
chr15:90308848..90308983hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608938
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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