A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741778



Internal ID165444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103424542..103441300hg38UCSC Ensembl
chrX:102679470..102696228hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3816759
hg1916759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741778
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000835596


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