A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1225n152



Internal ID22816928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1584716..1584782hg38UCSC Ensembl
chr11:1605946..1606012hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3197306, nsv3209260
SamplesHG00733, HG00514
Known GenesKRTAP5-1, KRTAP5-AS1, MOB2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1225n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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