A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445210



Internal ID21102763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90075283..90080789hg38UCSC Ensembl
chr9:92837565..92843071hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg385507
hg195507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445210
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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