A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181228



Internal ID22336472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52669160..52669325hg38UCSC Ensembl
chr4:53535327..53535492hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14466768
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3181228
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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