A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879335



Internal ID22654304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153977790..153978085hg38UCSC Ensembl
chrX:153243241..153243536hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439072
Samples
Known GenesTMEM187
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879335
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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