A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8873n152



Internal ID22824576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155733473..155733554hg38UCSC Ensembl
chr7:155526167..155526248hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3170471, nsv3179403
SamplesHG00733, HG00514
Known GenesRBM33
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8873n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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