A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658846



Internal ID21607151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95149205..95149205hg38UCSC Ensembl
chr12:95542981..95542981hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091785
SamplesHG00513
Known GenesFGD6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658846
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer