A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618725



Internal ID21567030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27995279..27995279hg38UCSC Ensembl
chrX:28013396..28013396hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166734
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618725
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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