A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738671



Internal ID162337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1018817..1342171hg38UCSC Ensembl
chrX:979552..1461064hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38323355
hg19481513
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557491
Supporting Variants
Samples
Known GenesCRLF2, CSF2RA, IL3RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738671
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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