A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610077



Internal ID21802124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41539411..41539473hg38UCSC Ensembl
chr15:41831609..41831671hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032834
Supporting Variants
Samples
Known GenesRPAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610077
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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