A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207660



Internal ID22356018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52707299..52707411hg38UCSC Ensembl
chr13:53281434..53281546hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14427054
SamplesHG00514
Known GenesLECT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207660
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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