A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv988n106



Internal ID22794816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67667322..67700171hg38UCSC Ensembl
chr13:68241454..68274303hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3832850
hg1932850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1140232, nsv1125281
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv988n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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