A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404778



Internal ID21062331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164110349..164124092hg38UCSC Ensembl
chr5:163537355..163551098hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3813744
hg1913744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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