A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615216



Internal ID21563521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160031488..160031488hg38UCSC Ensembl
chr3:159749275..159749275hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135900
SamplesHG03371
Known GenesIL12A-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615216
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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