A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148524



Internal ID19200771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62798875..62848676hg38UCSC Ensembl
Outerchr9:66454699..66504500hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3849802
hg1949802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000563
SamplesKWB1
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148524
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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