A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619794



Internal ID21568099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39933334..39933334hg38UCSC Ensembl
chrX:39792588..39792588hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167381
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619794
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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