A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455182



Internal ID22249653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42845977..42846122hg38UCSC Ensembl
chr3:42887469..42887614hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182904
Supporting Variants
SamplesHG00733
Known GenesACKR2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14455182
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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