A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17847842



Internal ID22031485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73794510..73794510hg38UCSC Ensembl
chr14:74261213..74261213hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241514
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17847842
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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