A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614538



Internal ID21562843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68807660..68807660hg38UCSC Ensembl
chrX:68027503..68027503hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg382352
hg192352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168134
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614538
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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