A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132713



Internal ID19281183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40771872..40835872hg38UCSC Ensembl
Outerchr9:66724900..66788900hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3864001
hg1964001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4031n106
Supporting Variantsnssv3987503
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132713
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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