A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566553



Internal ID21514881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56104642..56105110hg38UCSC Ensembl
chr8:57017201..57017669hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147022
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566553
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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