A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665513



Internal ID21613818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27800816..27802390hg38UCSC Ensembl
chrX:27818933..27820507hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166728
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665513
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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