A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447571



Internal ID21105124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86945001..86947100hg38UCSC Ensembl
chr9:89559916..89562015hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182013
Samples
Known GenesGAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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