A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190639



Internal ID22341474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49922963..49923108hg38UCSC Ensembl
chr14:50389681..50389826hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14445428
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)nsv3190639
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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