A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449107



Internal ID21106660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33586693..33589804hg38UCSC Ensembl
chr9:33586691..33589802hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383112
hg193112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449107
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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