A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999898



Internal ID21909241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43142099..43142277hg38UCSC Ensembl
chr5:43142201..43142379hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538486
Samples
Known GenesZNF131
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999898
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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