A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14411966



Internal ID22147502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134172951..134181050hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222808
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14411966
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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