A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766565



Internal ID20542425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105826266..105826323hg38UCSC Ensembl
chrX:105070259..105070316hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283657
Samples
Known GenesNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766565
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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