A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125028



Internal ID19249784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39865982..39880882hg38UCSC Ensembl
Outerchr9:42011000..42025900hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814901
hg1914901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977833
SamplesKWS2
Known GenesKGFLP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125028
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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