A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446454



Internal ID21104007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91402301..91428000hg38UCSC Ensembl
chr9:94164583..94190282hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3825700
hg1925700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234640
Samples
Known GenesNFIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446454
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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