A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881258



Internal ID22656233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153444816..153444872hg38UCSC Ensembl
chrX:152710274..152710330hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436910
Samples
Known GenesTREX2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881258
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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