A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736612



Internal ID160278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42887837..42909837hg38UCSC Ensembl
chrX:42747086..42769086hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428606
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736612
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00104471


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