A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17843882



Internal ID22027525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47797247..47797247hg38UCSC Ensembl
chr12:48191030..48191030hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241004
Supporting Variants
Samples
Known GenesHDAC7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17843882
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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