A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379973



Internal ID21037526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164482404..164550541hg38UCSC Ensembl
chr4:165403556..165471693hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3868138
hg1968138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213779
Samples
Known GenesMIR5684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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