A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565648



Internal ID21513962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3310321..3310379hg38UCSC Ensembl
chr6:3310555..3310613hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146664
SamplesNA19238
Known GenesSLC22A23
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565648
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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