A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442056



Internal ID21099609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65703901..65718500hg38UCSC Ensembl
chr9:42684821..42699420hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814600
hg1914600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7806n223
Supporting Variantsnssv18223199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer