A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384267



Internal ID21041820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43669701..43676000hg38UCSC Ensembl
chr4:43671718..43678017hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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