A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430578



Internal ID21088131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1143571..1432605hg38UCSC Ensembl
chr9:1143571..1432605hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38289035
hg19289035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430578
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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