A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17844281



Internal ID22027924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54461690..54461690hg38UCSC Ensembl
chr12:54855474..54855474hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241046
Supporting Variants
Samples
Known GenesGTSF1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17844281
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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