A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077811



Internal ID19325237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98000969..98002870hg38UCSC Ensembl
chr15:98544199..98546100hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766497
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077811
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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