A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984477



Internal ID21893820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61814548..61980438hg38UCSC Ensembl
chr1:62280220..62446110hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38165891
hg19165891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533778
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984477
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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