A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555911



Internal ID329060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46592209..46592278hg38UCSC Ensembl
chrX:46451644..46451713hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736758
Samples
Known GenesCHST7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555911
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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