A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439749



Internal ID22182057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66337937..66338003hg38UCSC Ensembl
chr9:42183748..42183802hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3867
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225613
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)nssv14439749
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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