A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847854



Internal ID22031497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74889697..74889697hg38UCSC Ensembl
chr14:75356400..75356400hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241526
Supporting Variants
Samples
Known GenesDLST
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847854
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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