A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116460



Internal ID18900982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:68441329..68831268hg38UCSC Ensembl
Outerchr14:68908046..69297985hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38389940
hg19389940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978641
SamplesKWS2
Known GenesRAD51B, ZFP36L1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116460
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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