A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154732



Internal ID21449933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25441354..25441792hg38UCSC Ensembl
chr6:25441582..25442020hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571201
Supporting Variants
SamplesHG01114
Known GenesLRRC16A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154732
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