A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114057



Internal ID21506154
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 StatusS
Merged Variantsnsv5612910
Supporting Variants
SamplesNA19983
Known GenesVIT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114057
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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