A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602776



Internal ID21794823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73644774..73644848hg38UCSC Ensembl
chr15:73937115..73937189hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022396
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602776
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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