A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180191



Internal ID22335948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41306200..41306260hg38UCSC Ensembl
chr3:41347691..41347751hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5947n152
Supporting Variantsnssv14450397
SamplesHG00733
Known GenesULK4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3180191
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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