A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581212



Internal ID21529708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166384240..166391932hg38UCSC Ensembl
chr6:166797728..166805420hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg387693
hg197693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149703
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581212
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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