A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215588



Internal ID20782628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13307593..13307931hg38UCSC Ensembl
chr6:13307825..13308163hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413950
Supporting Variants
Samples
Known GenesTBC1D7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215588
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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