A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611807



Internal ID21560112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25446172..25446172hg38UCSC Ensembl
chrX:25464289..25464289hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381833
hg191833
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167149
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611807
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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