A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437120



Internal ID21094673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97126795..97127935hg38UCSC Ensembl
chr9:99889077..99890217hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437120
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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