A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565864



Internal ID22434573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119168600..119168600hg38UCSC Ensembl
chr9:121930878..121930878hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349180, nssv14349182, nssv14349183, nssv14349181
SamplesHG00512, HG00733, HG00513, HG00514
Known GenesBRINP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565864
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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