A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599247



Internal ID21791292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95544203..95546280hg38UCSC Ensembl
chr15:96087432..96089509hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599247
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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