A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181958



Internal ID22336841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143500756..143502383hg38UCSC Ensembl
chr3:143219598..143221225hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381628
hg191628
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14410286
SamplesNA19240
Known GenesSLC9A9
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3181958
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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