A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623101



Internal ID21571406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22017868..22017868hg38UCSC Ensembl
chrX:22035986..22035986hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385035
hg195035
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166220
SamplesNA19240
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623101
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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