A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177178



Internal ID22334285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66131861..66131993hg38UCSC Ensembl
chr8:67044096..67044228hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14429632
SamplesHG00514
Known GenesTRIM55
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177178
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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