A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645246



Internal ID21593551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59209875..59209875hg38UCSC Ensembl
chr11:58977348..58977348hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075534
SamplesHG00732
Known GenesMPEG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645246
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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