A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110306



Internal ID21412990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15144049..15144049hg38UCSC Ensembl
chr2:15284173..15284173hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610903
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110306
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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