A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520542



Internal ID21844901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93837458..93840964hg38UCSC Ensembl
chr1:94303014..94306520hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg383507
hg193507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985464
Supporting Variants
Samples
Known GenesBCAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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