A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611762



Internal ID21803809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75120455..75120673hg38UCSC Ensembl
chr15:75412796..75413014hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611762
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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