A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571917



Internal ID21520300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23743031..23745716hg38UCSC Ensembl
chr6:23743259..23745944hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382686
hg192686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147588
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571917
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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