A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582031



Internal ID21530539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50484753..50485081hg38UCSC Ensembl
chr6:50452466..50452794hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155906
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582031
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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