A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14405861



Internal ID22296402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88546051..88548780hg38UCSC Ensembl
chr16:88612459..88615188hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208307
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14405861
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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