A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642085



Internal ID21590390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73660146..73660146hg38UCSC Ensembl
chr10:75419904..75419904hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071622
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642085
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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