A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381020



Internal ID22290673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135534367..135534428hg38UCSC Ensembl
chr9:138426213..138426274hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224204
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)nssv14381020
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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