A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436955



Internal ID21094508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120789901..120795900hg38UCSC Ensembl
chr9:123552179..123558178hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232735
Samples
Known GenesFBXW2, LOC100288842
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436955
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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