A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877933



Internal ID22652899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118920798..118922749hg38UCSC Ensembl
chrX:118054761..118056712hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg381952
hg191952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877933
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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