A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383223



Internal ID21040776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143163701..143173200hg38UCSC Ensembl
chr4:144084854..144094353hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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