A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981551



Internal ID21890894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159429373..159430370hg38UCSC Ensembl
chr1:159399163..159400160hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981551
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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