A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983841



Internal ID21893184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32750785..32751089hg38UCSC Ensembl
chr1:33216386..33216690hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523389
Samples
Known GenesKIAA1522
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983841
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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