A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190652



Internal ID20757692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97547835..97548261hg38UCSC Ensembl
chr9:100310117..100310543hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436026
Supporting Variants
Samples
Known GenesTMOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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