A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619262



Internal ID21567567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46380274..46380274hg38UCSC Ensembl
chrX:46239709..46239709hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167568
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619262
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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