A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415028



Internal ID21072581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3349821..3351722hg38UCSC Ensembl
chr6:3350055..3351956hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142840
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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