A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3539837



Internal ID22408990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168673563..168673563hg38UCSC Ensembl
chr6:169074102..169074102hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381730
hg191730
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456641
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)nsv3539837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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