A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523253



Internal ID21847612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151599299..151599550hg38UCSC Ensembl
chr1:151571775..151572026hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523253
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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