A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641137



Internal ID21589442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168309421..168309421hg38UCSC Ensembl
chr6:168710101..168710101hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159091, nssv17154640
SamplesHG00512, NA20847
Known GenesDACT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641137
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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