A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868284



Internal ID22643219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24126680..24127392hg38UCSC Ensembl
chrX:24144797..24145509hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453022
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868284
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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