A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14441473



Internal ID22237859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9364768..9367007hg38UCSC Ensembl
chr10:9406731..9408970hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382240
hg192240
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196064
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)nssv14441473
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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