A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573906



Internal ID21522315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101804524..101804607hg38UCSC Ensembl
chr8:102816752..102816835hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142962
SamplesNA19238
Known GenesNCALD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573906
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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