A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17845751



Internal ID22029394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21359600..21359600hg38UCSC Ensembl
chr14:21827759..21827759hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249664
Supporting Variants
Samples
Known GenesSUPT16H
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17845751
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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