A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111595



Internal ID21503688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225663674..225663674hg38UCSC Ensembl
chr2:226528390..226528390hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620307
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111595
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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