A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878325



Internal ID22653290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116950866..117201706hg38UCSC Ensembl
chrX:116084834..116335669hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38250841
hg19250836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878325
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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