A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476037



Internal ID253659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39079733..39079785hg38UCSC Ensembl
chr8:38937252..38937304hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009574
Samples
Known GenesADAM9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476037
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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