A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423988



Internal ID21081541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5820081..5822036hg38UCSC Ensembl
chr9:5820081..5822036hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381956
hg191956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220419
Samples
Known GenesERMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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