A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882046



Internal ID22657023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5443766..5445044hg38UCSC Ensembl
chrX:5361807..5363085hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg381279
hg191279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882046
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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