A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109224



Internal ID21402096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155232828..155232828hg38UCSC Ensembl
chr2:156089340..156089340hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622438
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109224
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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