A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147691



Internal ID19195892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:311114..311705hg38UCSC Ensembl
Outerchr16:361114..361705hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996479
SamplesKWB1
Known GenesAXIN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147691
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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