A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17855764



Internal ID22039407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10562382..10562382hg38UCSC Ensembl
chr1:10622439..10622439hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254476
Supporting Variants
Samples
Known GenesPEX14
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17855764
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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