A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854204



Internal ID22037847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120190454..120190454hg38UCSC Ensembl
chr3:119909301..119909301hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254593
Supporting Variants
Samples
Known GenesGPR156
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854204
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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