A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111597



Internal ID21503684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225782469..225782469hg38UCSC Ensembl
chr2:226647185..226647185hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605536
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111597
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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