A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531723



Internal ID21856079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35423431..35423537hg38UCSC Ensembl
chr1:35889032..35889138hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531723
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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