A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383292



Internal ID21040845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44772643..44790950hg38UCSC Ensembl
chr4:44774660..44792967hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3818308
hg1918308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383292
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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