A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620849



Internal ID21569154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95890219..95890219hg38UCSC Ensembl
chrX:95145218..95145218hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg381504
hg191504
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169292
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620849
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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