A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564980



Internal ID21513288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134282514..134283351hg38UCSC Ensembl
chr6:134603652..134604489hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151204
SamplesNA19238
Known GenesSGK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564980
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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