A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579946



Internal ID21528431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63857151..63857274hg38UCSC Ensembl
chr8:64769708..64769831hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141025
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579946
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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