A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960832



Internal ID18860665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:47484741..47486161hg38UCSC Ensembl
Outerchr11:47506293..47507713hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381421
hg191421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120085
Supporting Variants
SamplesKWS1
Known GenesCELF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960832
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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