A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078056



Internal ID18969837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33382101..33396102hg38UCSC Ensembl
chr9:33382099..33396100hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3814002
hg1914002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765976
SamplesKWP1
Known GenesAQP7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078056
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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