A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611091



Internal ID21559396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15481512..15481512hg38UCSC Ensembl
chr2:15621636..15621636hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109507
SamplesHG03486
Known GenesNBAS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611091
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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