A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189135



Internal ID22340619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53923793..53925220hg38UCSC Ensembl
chr4:54789960..54791387hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6606n152
Supporting Variantsnssv14425317, nssv14398386
SamplesNA19240, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3189135
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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