A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640732



Internal ID21589037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30987183..30987183hg38UCSC Ensembl
chr6:30954960..30954960hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154065
SamplesHG00732
Known GenesMUC21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640732
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