A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230779



Internal ID20797819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72795201..72857400hg38UCSC Ensembl
chr9:75410117..75472316hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3862200
hg1962200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436864
Supporting Variants
Samples
Known GenesTMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230779
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00064


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