A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180350



Internal ID22336024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41306200..41306261hg38UCSC Ensembl
chr3:41347691..41347752hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5947n152
Supporting Variantsnssv14423953
SamplesHG00514
Known GenesULK4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3180350
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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