A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389322



Internal ID21046875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39409436..39425656hg38UCSC Ensembl
chr4:39411056..39427276hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3816221
hg1916221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213579
Samples
Known GenesKLB, MIR1273H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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