A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078640



Internal ID19324764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62798875..62895376hg38UCSC Ensembl
chr9:66454699..66551200hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3896502
hg1996502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767154
SamplesKWP1
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078640
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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