A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111332



Internal ID22020565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1374860..1375325hg38UCSC Ensembl
chrX:1493753..1494218hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648494
Samples
Known GenesIL3RA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111332
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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