A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639560



Internal ID21587865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17849122..17849122hg38UCSC Ensembl
chr10:18138051..18138051hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg386228
hg196228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069480
SamplesHG00096
Known GenesMRC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639560
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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