A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560251



Internal ID333263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1113487..1380049hg38UCSC Ensembl
chrX:1213640..1498942hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38266563
hg19285303
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv555n206
Supporting Variantsnssv17738711
Samples
Known GenesCRLF2, CSF2RA, IL3RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560251
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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