A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551680



Internal ID21876035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128731767..128731914hg38UCSC Ensembl
chr3:128450610..128450757hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991123
Supporting Variants
Samples
Known GenesRAB7A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551680
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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