A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv577n106



Internal ID22794405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3663070..3663158hg38UCSC Ensembl
chr11:3684300..3684388hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1125520, nsv1111047
SamplesKWS2, KWS1
Known GenesART1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv577n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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