A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636661



Internal ID21584966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40491463..40491463hg38UCSC Ensembl
chr6:40459202..40459202hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154922
SamplesNA24385
Known GenesLRFN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636661
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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