A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566169



Internal ID21514491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106006388..106007519hg38UCSC Ensembl
chr6:106454263..106455394hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155240
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566169
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