A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633024



Internal ID21581329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68448940..68448940hg38UCSC Ensembl
chr10:70208697..70208697hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070917
SamplesHG00513
Known GenesDNA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633024
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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