A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426392



Internal ID21083945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29933901..30126300hg38UCSC Ensembl
chr9:29933899..30126298hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38192400
hg19192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426392
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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