A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657988



Internal ID21606293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75727030..75727030hg38UCSC Ensembl
chr11:75438075..75438075hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075893
SamplesNA20509
Known GenesMOGAT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657988
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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