A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448054



Internal ID21105607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116106203..116340508hg38UCSC Ensembl
chr9:118868482..119102787hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38234306
hg19234306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234967
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448054
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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