A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133064



Internal ID19274045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:68905256..68911470hg38UCSC Ensembl
Outerchr18:66572493..66578707hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg386215
hg196215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987873
SamplesKWS1
Known GenesCCDC102B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133064
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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