A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386898



Internal ID21044451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20914935..21068308hg38UCSC Ensembl
chr5:20915044..21068417hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38153374
hg19153374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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