A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152168



Internal ID19196666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:15326800..15338601hg38UCSC Ensembl
Outerchr18:15326799..15338600hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3811802
hg1911802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996772
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152168
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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