A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850099



Internal ID22033742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:124198778..124198778hg38UCSC Ensembl
chrX:123332628..123332628hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850099
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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