A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403909



Internal ID21061462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66494743..66509595hg38UCSC Ensembl
chr5:65790571..65805423hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3814853
hg1914853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133298
Samples
Known GenesLOC101928769
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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