A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883874



Internal ID22658856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116654129..116713057hg38UCSC Ensembl
chrX:115788097..115847025hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3858929
hg1958929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883874
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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