A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14401800



Internal ID22294164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7949357..7953143hg38UCSC Ensembl
chr9:7949357..7953143hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg383787
hg193787
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194525
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)nssv14401800
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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