A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103265



Internal ID22012498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153382541..153382743hg38UCSC Ensembl
chrX:152647999..152648201hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103265
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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