A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651982



Internal ID21600287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30917001..30917001hg38UCSC Ensembl
chr11:30938548..30938548hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074554
SamplesNA20847
Known GenesDCDC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651982
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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