A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417536



Internal ID21075089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19121462..19122112hg38UCSC Ensembl
chr9:19121460..19122110hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220523
Samples
Known GenesPLIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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