A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981507



Internal ID21890850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150915694..150923417hg38UCSC Ensembl
chr1:150888170..150895893hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg387724
hg197724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981507
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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