A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566743



Internal ID21515071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121474423..121479199hg38UCSC Ensembl
chr6:121795569..121800345hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384777
hg194777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142929
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566743
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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