A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432515



Internal ID21090068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30778975..30793087hg38UCSC Ensembl
chr8:30636491..30650603hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3814113
hg1914113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221143
Samples
Known GenesPPP2CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432515
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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