A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610757



Internal ID21559062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22700250..22700250hg38UCSC Ensembl
chrX:22718367..22718367hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166674
SamplesNA18939
Known GenesLOC100873065
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610757
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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