A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622336



Internal ID21570641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3560616..3560616hg38UCSC Ensembl
chr2:3608206..3608206hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381996
hg191996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113105
SamplesHG02587
Known GenesRNASEH1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622336
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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