A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617360



Internal ID21565665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9655467..9655467hg38UCSC Ensembl
chr2:9795596..9795596hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115322
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617360
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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