A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566837



Internal ID21515167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41897032..41897592hg38UCSC Ensembl
chr6:41864770..41865330hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148978
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566837
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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