A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436447



Internal ID21094000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97179512..97180247hg38UCSC Ensembl
chr9:99941794..99942529hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436447
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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