A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435651



Internal ID21093204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98234923..98235752hg38UCSC Ensembl
chr9:100997205..100998034hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189448
Samples
Known GenesTBC1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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