A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535147



Internal ID21859502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151112117..151112180hg38UCSC Ensembl
chr1:151084593..151084656hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981609
Supporting Variants
Samples
Known GenesGABPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535147
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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