A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961092



Internal ID19220204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:65676300..65676358hg38UCSC Ensembl
Outerchr11:65443771..65443829hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110684
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961092
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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