A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151207



Internal ID19201665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:92764239..92779477hg38UCSC Ensembl
Outerchr14:93230584..93245822hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3815239
hg1915239
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002141
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151207
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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