A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364028



Internal ID21021581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12887563..12887998hg38UCSC Ensembl
chr4:12889187..12889622hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364028
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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