A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881192



Internal ID22656166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:356823..356935hg38UCSC Ensembl
chrX:317558..317670hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463374
Samples
Known GenesPPP2R3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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