A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383106



Internal ID21040659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113896901..113902100hg38UCSC Ensembl
chr4:114818057..114823256hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106309
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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