A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1n106



Internal ID22793829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11100..29200hg38UCSC Ensembl
chr1:11100..29200hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3818101
hg1918101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1141121, nsv1118423
SamplesKWS2, KWS1
Known GenesDDX11L1, MIR6859-1, MIR6859-2, WASH7P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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