A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961038



Internal ID19208822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110954997..110955053hg38UCSC Ensembl
Outerchr11:110825721..110825777hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120249
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961038
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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