A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738682



Internal ID162348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1060846..1290182hg38UCSC Ensembl
chrX:1021581..1409075hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38229337
hg19387495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424837
Supporting Variants
Samples
Known GenesCRLF2, CSF2RA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738682
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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