A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849216



Internal ID22032859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46380355..46380355hg38UCSC Ensembl
chrX:46239790..46239790hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849216
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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