A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103084



Internal ID22012317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153684742..153685135hg38UCSC Ensembl
chrX:152950197..152950590hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103084
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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