A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962246



Internal ID19217156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3663070..3663136hg38UCSC Ensembl
Outerchr11:3684300..3684366hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111047
Supporting Variants
SamplesKWS1
Known GenesART1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962246
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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