A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078068



Internal ID19320373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62348198..62356299hg38UCSC Ensembl
chr9:46659499..46667600hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388102
hg198102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768215
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078068
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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