A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884569



Internal ID22659552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:124471146..124471558hg38UCSC Ensembl
chrX:123604996..123605408hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437838
Samples
Known GenesTENM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884569
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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