A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981830



Internal ID21891173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172420186..172427116hg38UCSC Ensembl
chr1:172389326..172396256hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg386931
hg196931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524842
Samples
Known GenesC1orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981830
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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