A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741868



Internal ID165534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107592724..107592732hg38UCSC Ensembl
chrX:106835954..106835962hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741868
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.017101


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