A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183269



Internal ID22337535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164192233..164192432hg38UCSC Ensembl
chr6:164613265..164613464hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14427104
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)nsv3183269
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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