A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110945



Internal ID19255726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:17675246..17690514hg38UCSC Ensembl
Outerchr3:17716738..17732006hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3815269
hg1915269
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961367
SamplesKWS1
Known GenesTBC1D5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110945
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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