A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187790



Internal ID22339910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55628218..55628268hg38UCSC Ensembl
chr3:55662246..55662296hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14423485
SamplesHG00514
Known GenesERC2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187790
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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