A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143414



Internal ID20710454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43197208..43197645hg38UCSC Ensembl
chr6:43164946..43165383hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399930
Supporting Variants
Samples
Known GenesCUL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00351


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