A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178148



Internal ID22334828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144345099..144345207hg38UCSC Ensembl
chr6:144666235..144666343hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463667
SamplesHG00733
Known GenesUTRN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178148
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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