A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv580n106



Internal ID22794408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5763270..5788070hg38UCSC Ensembl
chr11:5784500..5809300hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824801
hg1924801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1130199, nsv1130303
SamplesKWS2, KWS1
Known GenesOR52N1, OR52N5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv580n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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