A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610883



Internal ID21559188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162936686..162936686hg38UCSC Ensembl
chr2:163793196..163793196hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109610, nssv17109613, nssv17109611, nssv17109612
SamplesHG03065, NA19238, HG00731, NA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610883
Frequency
Sample Size35
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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