A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3185793



Internal ID22338852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110031681..110031773hg38UCSC Ensembl
chr6:110352884..110352976hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14400491
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3185793
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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