A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563456



Internal ID22432192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28922219..28922219hg38UCSC Ensembl
chr4:28923841..28923841hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313278, nssv14313279
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563456
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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