A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175142



Internal ID22333197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25882639..25882867hg38UCSC Ensembl
chr6:25882867..25883095hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456897
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175142
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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