A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416893



Internal ID21074446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9091246..9099258hg38UCSC Ensembl
chr9:9091246..9099258hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg388013
hg198013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234811
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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