A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968252



Internal ID22743188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152793394..152830633hg38UCSC Ensembl
chrX:151961938..151999177hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3837240
hg1937240
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515642
Samples
Known GenesCETN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968252
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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