A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2009n106



Internal ID22795837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118771208..118773043hg38UCSC Ensembl
chr2:119528784..119530619hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1141859, nsv1125291
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2009n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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