A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075945



Internal ID19317100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39800835..39803536hg38UCSC Ensembl
chr18:37380799..37383500hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769463
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075945
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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