A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144831



Internal ID20711871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5769597..5779042hg38UCSC Ensembl
chr6:5769830..5779275hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg389446
hg199446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406376
Supporting Variants
Samples
Known GenesFARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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