A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732374



Internal ID20508298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16830829..16830829hg38UCSC Ensembl
chrX:16848952..16848952hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281137
Samples
Known GenesTXLNG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732374
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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