A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455158



Internal ID21112711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98061068..98061721hg38UCSC Ensembl
chr9:100823350..100824003hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187874
Samples
Known GenesNANS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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