A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563771



Internal ID22432507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42326676..42326676hg38UCSC Ensembl
chr4:42328693..42328693hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313086
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563771
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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