A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610362



Internal ID21558667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97185527..97185527hg38UCSC Ensembl
chrX:96440526..96440526hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168806
SamplesHG00864
Known GenesDIAPH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610362
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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