A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14442800



Internal ID22228584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19421027..19421291hg38UCSC Ensembl
chr11:19442574..19442838hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196126
Supporting Variants
SamplesHG00733
Known GenesNAV2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14442800
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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