A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv564n106



Internal ID20159921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:389168..574449hg38UCSC Ensembl
chr11:389168..574449hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38185282
hg19185282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1116453, nsv1110854
SamplesKWS2, KWS1
Known GenesANO9, C11orf35, HRAS, LOC143666, LRRC56, MIR210, MIR210HG, PKP3, PTDSS2, RASSF7, RNH1, SIGIRR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv564n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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