A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765898



Internal ID20541758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3691429..3691484hg38UCSC Ensembl
chrX:3609470..3609525hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288984
Samples
Known GenesPRKX
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765898
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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