A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845878



Internal ID22029521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50794701..50794701hg38UCSC Ensembl
chr14:51261419..51261419hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6258854
Supporting Variants
Samples
Known GenesNIN
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845878
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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