A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851875



Internal ID22035518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104153291..104153291hg38UCSC Ensembl
chrX:103397972..103397972hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259669
Supporting Variants
Samples
Known GenesSLC25A53
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851875
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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