A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886630



Internal ID22661619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55076533..55090390hg38UCSC Ensembl
chrX:55102966..55116823hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3813858
hg1913858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462473
Samples
Known GenesPAGE2, PAGE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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