A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv27n97



Internal ID22815424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248561933..248662519hg38UCSC Ensembl
chr1:248725234..248825820hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38100587
hg19100587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155000, nsv1155107, nsv1155109, nsv1155108, nsv1155106
Samples
Known GenesOR2T10, OR2T11, OR2T27, OR2T34, OR2T35
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv27n97
Frequency
Sample Size131
Observed Gain0
Observed Loss39
Observed Complex0
Frequencyn/a


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