A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205034



Internal ID22353736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982123..60982173hg38UCSC Ensembl
chr11:60749595..60749645hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1405n152
Supporting Variantsnssv14377715, nssv14441628
SamplesNA19240, HG00733
Known GenesCD6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205034
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer