A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219165



Internal ID20786205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99276951..99296464hg38UCSC Ensembl
chr6:99724827..99744340hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3819514
hg1919514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617364
Supporting Variants
Samples
Known GenesFAXC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219165
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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