A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767154



Internal ID19315689
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 StatusS
Merged Variantsnsv1078640
Supporting Variants
SamplesKWP1
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767154
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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