A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368284



Internal ID21025837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28702892..28781118hg38UCSC Ensembl
chr4:28704514..28782740hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3878227
hg1978227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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