A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433037



Internal ID211763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1215504..1362856hg38UCSC Ensembl
chrX:1334397..1481749hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38147353
hg19147353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738744
Samples
Known GenesCSF2RA, IL3RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433037
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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