A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14404590



Internal ID22313446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36662441..36662493hg38UCSC Ensembl
chr15:36954642..36954694hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190591
Supporting Variants
SamplesNA19240
Known GenesC15orf41
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14404590
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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