A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563457



Internal ID22432193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3051815..3051815hg38UCSC Ensembl
chr4:3053542..3053542hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309895
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563457
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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