A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3542848



Internal ID22411916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160857480..160857480hg38UCSC Ensembl
chr6:161278512..161278512hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463401
SamplesHG00733
Known Genes
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)nsv3542848
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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