A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981461



Internal ID21890804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15510033..15510101hg38UCSC Ensembl
chr1:15836528..15836596hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519838
Samples
Known GenesCASP9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981461
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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