A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879896



Internal ID22654866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23806214..23808999hg38UCSC Ensembl
chrX:23824331..23827116hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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