A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610787



Internal ID21559092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118094013..118094013hg38UCSC Ensembl
chr2:118851589..118851589hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17108264
SamplesHG00513
Known GenesINSIG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610787
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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