A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543183



Internal ID21867538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171908369..171908847hg38UCSC Ensembl
chr4:172829520..172829998hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5996512
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543183
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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