A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180934



Internal ID22336317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197030147..197030231hg38UCSC Ensembl
chr3:196757018..196757102hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14410379
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)nsv3180934
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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