A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449483



Internal ID21107036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104199826..104382315hg38UCSC Ensembl
chr9:106962107..107144596hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38182490
hg19182490
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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