A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14444545



Internal ID22240519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60801550..60801828hg38UCSC Ensembl
chr15:61093749..61094027hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210173
Supporting Variants
SamplesHG00733
Known GenesRORA
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14444545
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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