A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614824



Internal ID21563129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115436030..115436030hg38UCSC Ensembl
chrX:114670492..114670492hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164752
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614824
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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