A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14423902



Internal ID22163068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32953575..32953654hg38UCSC Ensembl
chr3:32995067..32995146hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3175309
Supporting Variants
SamplesHG00514
Known GenesCCR4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14423902
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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