A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384195



Internal ID21041748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67845101..67846500hg38UCSC Ensembl
chr4:68710819..68712218hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211637
Samples
Known GenesTMPRSS11D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384195
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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