A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645732



Internal ID21594037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65540703..65540703hg38UCSC Ensembl
chr11:65308174..65308174hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075285
SamplesNA20847
Known GenesLTBP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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