A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407290



Internal ID21064843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88981870..89050325hg38UCSC Ensembl
chr5:88277687..88346142hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3868456
hg1968456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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