A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14408547



Internal ID22291187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62813332..62813392hg38UCSC Ensembl
chr20:61444684..61444744hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199281
Supporting Variants
SamplesNA19240
Known GenesOGFR
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14408547
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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