A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618789



Internal ID21567094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106174436..106174436hg38UCSC Ensembl
chrX:105418429..105418429hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164671
SamplesHG03125
Known GenesMUM1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618789
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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