A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528506



Internal ID21852863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33059581..33064886hg38UCSC Ensembl
chr1:33525182..33530487hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385306
hg195306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528506
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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