A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583522



Internal ID21532049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150322298..150326704hg38UCSC Ensembl
chr6:150643434..150647840hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384407
hg194407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148716
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583522
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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