A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644267



Internal ID21592572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90971183..90971183hg38UCSC Ensembl
chr10:92730940..92730940hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg382492
hg192492
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072253
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644267
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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