A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558368



Internal ID22427171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86615915..86636117hg38UCSC Ensembl
chr1:87081598..87101800hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3820203
hg1920203
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377231, nssv14378161, nssv14380455
SamplesHG00512, HG00513, HG00514
Known GenesCLCA3P
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558368
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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