A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286139



Internal ID20495357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153382526..153384462hg38UCSC Ensembl
chrX:152647984..152649920hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381937
hg191937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766283
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286139
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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