A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651768



Internal ID21600073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2137536..2137536hg38UCSC Ensembl
chr11:2158766..2158766hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382498
hg192498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073434
SamplesHG03009
Known GenesIGF2, INS-IGF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651768
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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