A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392338



Internal ID21049891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100973641..100980049hg38UCSC Ensembl
chr4:101894798..101901206hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386409
hg196409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392338
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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