A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146871



Internal ID20713911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93741168..93741611hg38UCSC Ensembl
chr6:94450886..94451329hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405914
Supporting Variants
Samples
Known GenesTSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00073


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