A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642034



Internal ID21590339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113490510..113490510hg38UCSC Ensembl
chr10:115250269..115250269hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068339
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642034
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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