A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612152



Internal ID21560457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6533375..6533375hg38UCSC Ensembl
chrX:6451416..6451416hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg382669
hg192669
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168240
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612152
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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