A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3189441



Internal ID22340784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156724416..156724874hg38UCSC Ensembl
chr3:156442205..156442663hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14423569
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3189441
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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