A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581897



Internal ID21530402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47546122..47547643hg38UCSC Ensembl
chr8:48458684..48460205hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381522
hg191522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147582
SamplesHG03486
Known GenesSPIDR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581897
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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