A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3939n106



Internal ID20163296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11100..39200hg38UCSC Ensembl
chr9:11100..39200hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3828101
hg1928101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1115797, nsv1119253
SamplesKWS2, KWS1
Known GenesDDX11L5, FAM138C, WASH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3939n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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