A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625277



Internal ID21573582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112224258..112224258hg38UCSC Ensembl
chr10:113984016..113984016hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068513
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625277
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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