A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281137



Internal ID20490355
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 StatusS
Merged Variantsnsv4732374
Supporting Variants
Samples
Known GenesTXLNG
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281137
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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