A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445693



Internal ID21103246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89538401..89540100hg38UCSC Ensembl
chr9:92153316..92155015hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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