A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642583



Internal ID21590888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8985436..8985436hg38UCSC Ensembl
chr10:9027399..9027399hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072229
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642583
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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