A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198386



Internal ID22348115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982123..60982174hg38UCSC Ensembl
chr11:60749595..60749646hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1405n152
Supporting Variantsnssv14414389
SamplesHG00514
Known GenesCD6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198386
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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