A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850134



Internal ID22033777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133392667..133392667hg38UCSC Ensembl
chrX:132526695..132526695hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242970
Supporting Variants
Samples
Known GenesGPC4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850134
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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