A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406346



Internal ID21063899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15460992..15466017hg38UCSC Ensembl
chr6:15461223..15466248hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385026
hg195026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139729
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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