A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581647



Internal ID21530149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42851733..42852490hg38UCSC Ensembl
chr3:42893225..42893982hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135768
SamplesNA19239
Known GenesACKR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581647
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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