A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563400



Internal ID22432137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154189481..154189481hg38UCSC Ensembl
chr4:155110633..155110633hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14319029, nssv14319028, nssv14319031, nssv14319027, nssv14319030, nssv14319032
SamplesHG00512, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563400
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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