A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854069



Internal ID22037712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72422376..72422376hg38UCSC Ensembl
chr3:72471527..72471527hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254192
Supporting Variants
Samples
Known GenesRYBP
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854069
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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