A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107540



Internal ID21494295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112732316..112732316hg38UCSC Ensembl
chr2:113489893..113489893hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622097
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107540
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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