A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876668



Internal ID22651629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115566419..115566713hg38UCSC Ensembl
chrX:114800742..114801035hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38295
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443553
Samples
Known GenesPLS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876668
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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