A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645648



Internal ID21593953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36055116..36055116hg38UCSC Ensembl
chr11:36076666..36076666hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074375
SamplesHG00731
Known GenesLDLRAD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645648
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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