A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521423



Internal ID21845782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114804430..114804569hg38UCSC Ensembl
chr1:115347051..115347190hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521423
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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