A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205685



Internal ID22354347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64822403..64822546hg38UCSC Ensembl
chr14:65289121..65289264hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2643n152
Supporting Variantsnssv14380999
SamplesNA19240
Known GenesSPTB
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205685
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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