A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181946



Internal ID22336834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197031523..197035943hg38UCSC Ensembl
chr3:196758394..196762814hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg384421
hg194421
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6346n152
Supporting Variantsnssv14463281, nssv14452922
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3181946
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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