A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611052



Internal ID21559357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127777012..127777012hg38UCSC Ensembl
chr3:127495855..127495855hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135927
SamplesNA19239
Known GenesMGLL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611052
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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