A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445706



Internal ID21103259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129955328..130102474hg38UCSC Ensembl
chr9:132717607..132864753hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38147147
hg19147147
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228165
Samples
Known GenesFNBP1, GPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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