A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542999



Internal ID21867354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4632503..4632954hg38UCSC Ensembl
chr4:4634230..4634681hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997334
Supporting Variants
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542999
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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