A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153345



Internal ID19203325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14182100..14185201hg38UCSC Ensembl
Outerchr18:14182099..14185200hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001260
SamplesKWB1
Known GenesANKRD20A5P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153345
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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