A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489966



Internal ID267231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:939019..939869hg38UCSC Ensembl
chr8:889019..889869hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38851
hg19851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007945
Samples
Known GenesERICH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489966
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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