A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565183



Internal ID21513494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111882647..111882964hg38UCSC Ensembl
chr6:112203850..112204167hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143677
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565183
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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