A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663234



Internal ID21611539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12330798..12330798hg38UCSC Ensembl
chr11:12352345..12352345hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073043
SamplesNA19239
Known GenesMICALCL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663234
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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