A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634728



Internal ID21583033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76639188..76639188hg38UCSC Ensembl
chr10:78398946..78398946hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071409
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634728
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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