A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450662



Internal ID21108215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127577501..127600094hg38UCSC Ensembl
chr9:130339780..130362373hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3822594
hg1922594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234948
Samples
Known GenesFAM129B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450662
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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