A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567066



Internal ID21515397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123859925..123866006hg38UCSC Ensembl
chr8:124872165..124878246hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg386082
hg196082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141993
SamplesHG02818
Known GenesFER1L6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567066
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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