A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614346



Internal ID21806393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41540349..41540414hg38UCSC Ensembl
chr15:41832547..41832612hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030460
Supporting Variants
Samples
Known GenesRPAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614346
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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