A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886594



Internal ID22661583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101836460..101836546hg38UCSC Ensembl
chrX:101091432..101091518hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439530
Samples
Known GenesNXF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886594
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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