A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3185753



Internal ID22338834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42936148..42936224hg38UCSC Ensembl
chr6:42903886..42903962hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14400404
SamplesNA19240
Known GenesCNPY3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3185753
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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