A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142865



Internal ID342066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:148000..734000hg38UCSC Ensembl
chr8:98000..684000hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38586001
hg19586001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007055
Samples
Known GenesERICH1, FAM87A, FBXO25, OR4F21, RPL23AP53, TDRP, ZNF596
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142865
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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