A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582408



Internal ID21530920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168283970..168284036hg38UCSC Ensembl
chr6:168684650..168684716hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146083
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582408
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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