A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146664



Internal ID19199291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:667545..667625hg38UCSC Ensembl
Outerchr18:667545..667625hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995822
SamplesKWB1
Known GenesTYMS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146664
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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