A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429168



Internal ID21086721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9140498..9162754hg38UCSC Ensembl
chr8:8998008..9020264hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3822257
hg1922257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234519
Samples
Known GenesPPP1R3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429168
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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