A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851701



Internal ID22035344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149263952..149263952hg38UCSC Ensembl
chrX:148345482..148345482hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851701
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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