A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411767



Internal ID22469637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174870828..174870916hg38UCSC Ensembl
chr3:174588618..174588706hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889332
Supporting Variants
Samples
Known GenesNAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411767
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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