A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621991



Internal ID21570296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64870536..64870536hg38UCSC Ensembl
chr3:64856211..64856211hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125325
SamplesHG02818
Known GenesADAMTS9-AS2, MIR548A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621991
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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