A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409352



Internal ID21066905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24901522..24903452hg38UCSC Ensembl
chr6:24901750..24903680hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381931
hg191931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140675
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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