A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441299



Internal ID21098852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116338248..116377468hg38UCSC Ensembl
chr9:119100527..119139747hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3839221
hg1939221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222999
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441299
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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