A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867741



Internal ID22642677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123804231..123806600hg38UCSC Ensembl
chrX:122938081..122940450hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg382370
hg192370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867741
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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