A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520807



Internal ID21845166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1532888..1532948hg38UCSC Ensembl
chr1:1468268..1468328hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981456
Supporting Variants
Samples
Known GenesATAD3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520807
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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