A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767546



Internal ID20543406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233763..47233817hg38UCSC Ensembl
chrX:47093162..47093216hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261696
Samples
Known GenesUSP11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767546
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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