A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14451084



Internal ID22246170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31125926..31126506hg38UCSC Ensembl
chr3:31167418..31167998hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174400
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)nssv14451084
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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