A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444447



Internal ID21102000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90313677..90316587hg38UCSC Ensembl
chr9:93075959..93078869hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382911
hg192911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444447
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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