A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174892



Internal ID22333063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165664136..165664242hg38UCSC Ensembl
chr4:166585288..166585394hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14424989
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)nsv3174892
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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