A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129324



Internal ID19276976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:90688803..92075847hg38UCSC Ensembl
Outerchr11:90421971..91809013hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381387045
hg191387043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962757
SamplesKWS1
Known GenesDISC1FP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129324
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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