A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529723



Internal ID21854080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55965963..55976397hg38UCSC Ensembl
chr1:56431636..56442070hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3810435
hg1910435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5984625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529723
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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