A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201422



Internal ID22350734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101723090..101726052hg38UCSC Ensembl
chr14:102189427..102192389hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382963
hg192963
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453305, nssv14467371
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)nsv3201422
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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