A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579463



Internal ID21527944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11466423..11466483hg38UCSC Ensembl
chr8:11323932..11323992hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148277
SamplesHG02818
Known GenesFAM167A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579463
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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