A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520493



Internal ID21844852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182693820..182699592hg38UCSC Ensembl
chr1:182662955..182668727hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385773
hg195773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520493
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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