A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741696



Internal ID165362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100724910..100774496hg38UCSC Ensembl
chrX:99979898..100029485hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3849587
hg1949588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416089
Supporting Variants
Samples
Known GenesSYTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00062435


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