A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454074



Internal ID22248718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61218819..61219079hg38UCSC Ensembl
chr9:43601404..43601924hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38261
hg19521
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209674
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454074
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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