A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610336



Internal ID21558641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109235901..109235901hg38UCSC Ensembl
chr2:109852357..109852357hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107356
SamplesNA24385
Known GenesSH3RF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610336
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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