A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610202



Internal ID21558507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9304597..9304597hg38UCSC Ensembl
chrX:9272637..9272637hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168974
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610202
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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