A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612910



Internal ID21561215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36701022..36701022hg38UCSC Ensembl
chr2:36928165..36928165hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114057
SamplesNA19983
Known GenesVIT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612910
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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