A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028435



Internal ID21937778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41539915..41539995hg38UCSC Ensembl
chr15:41832113..41832193hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611507
Samples
Known GenesRPAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028435
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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