A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563562



Internal ID22432298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28520965..28520965hg38UCSC Ensembl
chr4:28522587..28522587hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14313273, nssv14313274, nssv14313272
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563562
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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