A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389493



Internal ID21047046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9681959..9688233hg38UCSC Ensembl
chr5:9682071..9688345hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg386275
hg196275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135682
Samples
Known GenesLOC285692
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389493
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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