A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078088



Internal ID19320380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68238683..68243384hg38UCSC Ensembl
chr9:70853599..70858300hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg384702
hg194702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762594
SamplesKWP1
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078088
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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