A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377110



Internal ID22327722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79987000..79987058hg38UCSC Ensembl
chr9:82601915..82601973hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225157
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)nssv14377110
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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