A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv730n106



Internal ID20160087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117134526..117210019hg38UCSC Ensembl
chr11:117005242..117080735hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3875494
hg1975494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1116457, nsv1133003
SamplesKWS2, KWS1
Known GenesLOC100652768, PAFAH1B2, PCSK7, SIDT2, TAGLN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv730n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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