A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447965



Internal ID21105518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69759301..69762200hg38UCSC Ensembl
chr9:72374217..72377116hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223625
Samples
Known GenesPTAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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