A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1089n106



Internal ID22794917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60447277..60474610hg38UCSC Ensembl
chr14:60913995..60941328hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3827334
hg1927334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1125306, nsv1110858
SamplesKWS2, KWS1
Known GenesC14orf39
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1089n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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