A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622097



Internal ID21570402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112732316..112732316hg38UCSC Ensembl
chr2:113489893..113489893hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107541, nssv17107540
SamplesNA19238, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622097
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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