A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078418



Internal ID19317704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10001..26700hg38UCSC Ensembl
chr18:9999..26700hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3816700
hg1916702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764238
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078418
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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