A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3537596



Internal ID22406798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83145215..83145215hg38UCSC Ensembl
chr6:83854934..83854934hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14452848
SamplesHG00733
Known GenesDOPEY1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3537596
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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