A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981472



Internal ID21890815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157186095..157187020hg38UCSC Ensembl
chr1:157155885..157156810hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38926
hg19926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536408
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981472
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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