A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571346



Internal ID21519723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13882318..13883620hg38UCSC Ensembl
chr6:13882549..13883851hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149350
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571346
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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