A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611500



Internal ID21559805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85568237..85568237hg38UCSC Ensembl
chrX:84823242..84823242hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg381653
hg191653
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168914
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611500
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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