A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850972



Internal ID22034615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164533936..164533936hg38UCSC Ensembl
chr2:165390446..165390446hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243383
Supporting Variants
Samples
Known GenesGRB14
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850972
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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