A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981130



Internal ID21890473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150054632..150056373hg38UCSC Ensembl
chr1:150026614..150028362hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg381742
hg191749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981130
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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