A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995830



Internal ID21905173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:172658155..172658466hg38UCSC Ensembl
chr4:173579306..173579617hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550633
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995830
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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