A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430807



Internal ID21088360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29572445..29813249hg38UCSC Ensembl
chr9:29572443..29813247hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38240805
hg19240805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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