A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261696



Internal ID20470914
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 StatusS
Merged Variantsnsv4767546
Supporting Variants
Samples
Known GenesUSP11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261696
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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