A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451144



Internal ID22246226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108720098..108720503hg38UCSC Ensembl
chr3:108438945..108439350hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179327
Supporting Variants
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)nssv14451144
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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