A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738612



Internal ID162278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:833418..1344160hg38UCSC Ensembl
chrX:794153..1463053hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38510743
hg19668901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432954
Supporting Variants
Samples
Known GenesCRLF2, CSF2RA, IL3RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738612
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00457856


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