A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523314



Internal ID21847673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226086828..226108540hg38UCSC Ensembl
chr1:226274529..226296241hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3821713
hg1921713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523314
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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