A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598181



Internal ID21790225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64744895..64744970hg38UCSC Ensembl
chr15:65037094..65037169hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031045
Supporting Variants
Samples
Known GenesRBPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598181
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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