A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449225



Internal ID21106778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65474201..65515700hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3841500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7798n223
Supporting Variantsnssv18185868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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