A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659035



Internal ID21607340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79612617..79612617hg38UCSC Ensembl
chr12:80006397..80006397hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg382982
hg192982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087439
SamplesNA19650
Known GenesPAWR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659035
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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