A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389566



Internal ID21047119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153337701..153349000hg38UCSC Ensembl
chr4:154258853..154270152hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5524n223
Supporting Variantsnssv18212110
Samples
Known GenesMND1, TRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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