A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739674



Internal ID163340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23286001..23286101hg38UCSC Ensembl
chrX:23304118..23304218hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417329
Supporting Variants
Samples
Known GenesLOC100873065
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739674
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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