A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662806



Internal ID21611111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14626135..14626135hg38UCSC Ensembl
chr11:14647681..14647681hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg386105
hg196105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073718
SamplesHG02818
Known GenesPSMA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662806
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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