A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430201



Internal ID21087754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19427684..19497496hg38UCSC Ensembl
chr9:19427682..19497494hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3869813
hg1969813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226589
Samples
Known GenesACER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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