A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563485



Internal ID22432221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7752960..7752960hg38UCSC Ensembl
chr4:7754687..7754687hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311302, nssv14311298, nssv14311300, nssv14311303, nssv14311301, nssv14311297, nssv14311299
SamplesNA19238, NA19239, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563485
Frequency
Sample Size9
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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