A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3417n106



Internal ID20162774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154125780..154126105hg38UCSC Ensembl
chr6:154446915..154447240hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135663, nsv1111710, nsv1131596
SamplesKWS2, KWS1
Known GenesOPRM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3417n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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