A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960572



Internal ID19207824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:109078373..109084473hg38UCSC Ensembl
Outerchr11:108949100..108955200hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg386101
hg196101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128659
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960572
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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