A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006750



Internal ID20573790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100607526..100607691hg38UCSC Ensembl
chr13:101259780..101259945hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478131
Supporting Variants
Samples
Known GenesTMTC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006750
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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