A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140299



Internal ID19270779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:38909969..38910031hg38UCSC Ensembl
Outerchr13:39484106..39484168hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979008
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140299
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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