A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417393



Internal ID21074946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27884903..27931792hg38UCSC Ensembl
chr9:27884901..27931790hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3846890
hg1946890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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