A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189353



Internal ID22340729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2627388..2627528hg38UCSC Ensembl
chr4:2629115..2629255hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14454325, nssv14434704
SamplesHG00733, HG00514
Known GenesFAM193A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3189353
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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