A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438045



Internal ID21095598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130038729..130041432hg38UCSC Ensembl
chr9:132801008..132803711hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382704
hg192704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236908
Samples
Known GenesFNBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438045
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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