A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189900



Internal ID22341016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14523506..14525962hg38UCSC Ensembl
chr6:14523737..14526193hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382457
hg192457
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7752n152
Supporting Variantsnssv14425926
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3189900
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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