A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406875



Internal ID21064428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73688889..73704716hg38UCSC Ensembl
chr5:72984714..73000541hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3815828
hg1915828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216330
Samples
Known GenesARHGEF28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406875
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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