A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449267



Internal ID21106820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90793719..90816077hg38UCSC Ensembl
chr9:93556001..93578359hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3822359
hg1922359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217757
Samples
Known GenesSYK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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