A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134706



Internal ID20701746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105451339..105451926hg38UCSC Ensembl
chr6:105899214..105899801hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615638
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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