A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8855n152



Internal ID22824558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154645855..154672108hg38UCSC Ensembl
chr7:154437565..154463818hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3826254
hg1926254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3221851, nsv3217521
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, HG00733, HG00514
Known GenesDPP6
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8855n152
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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