A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980557



Internal ID21889900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104541052..105108572hg38UCSC Ensembl
chr1:105083674..105651194hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38567521
hg19567521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980557
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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