A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176095



Internal ID22333709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32663151..32663243hg38UCSC Ensembl
chr6:32630928..32631020hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7841n152
Supporting Variantsnssv14399239
SamplesNA19240
Known GenesHLA-DQB1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176095
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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