A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1637n152



Internal ID22817340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131679409..131682818hg38UCSC Ensembl
chr11:131549303..131552712hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198910, nsv3208872
SamplesNA19240, HG00733, 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)dgv1637n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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