A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208872



Internal ID22357040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131679409..131682633hg38UCSC Ensembl
chr11:131549303..131552527hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383225
hg193225
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1637n152
Supporting Variantsnssv14446036, nssv14419740, nssv14419739, nssv14446037
SamplesHG00733, HG00514
Known GenesNTM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208872
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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