A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451143



Internal ID22220142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108653665..108653787hg38UCSC Ensembl
chr3:108372512..108372634hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3177348
Supporting Variants
SamplesHG00733
Known GenesDZIP3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14451143
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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