A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455296



Internal ID22249750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73191319..73191503hg38UCSC Ensembl
chr15:73483660..73483844hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200323
Supporting Variants
SamplesHG00733
Known GenesNEO1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14455296
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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