A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111881



Internal ID21460370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233340751..233340751hg38UCSC Ensembl
chr2:234249397..234249397hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg388816
hg198816
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610906
Supporting Variants
SamplesHG02818
Known GenesSAG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111881
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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