A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1314n106



Internal ID22795142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20566628..20566714hg38UCSC Ensembl
chr16:20577950..20578036hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1125367, nsv1133055
SamplesKWS2, KWS1
Known GenesACSM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1314n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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