A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv970n106



Internal ID22794798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50278804..50301955hg38UCSC Ensembl
chr13:50852940..50876091hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3823152
hg1923152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1110898, nsv1116504
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv970n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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