A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849181



Internal ID22032824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38657313..38657313hg38UCSC Ensembl
chrX:38516566..38516566hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259424
Supporting Variants
Samples
Known GenesTSPAN7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849181
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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