A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422127



Internal ID21079680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30878090..30893071hg38UCSC Ensembl
chr9:30878088..30893069hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3814982
hg1914982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422127
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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