A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141609



Internal ID19283922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40463482..40467282hg38UCSC Ensembl
Outerchr9:42608500..42612300hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383801
hg193801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993114
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141609
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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