A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544156



Internal ID21868511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43159571..43160051hg38UCSC Ensembl
chr5:43159673..43160153hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999899
Supporting Variants
Samples
Known GenesZNF131
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544156
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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