A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4057n106



Internal ID22797885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65659774..65688645hg38UCSC Ensembl
chr9:70477400..70506300hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3828872
hg1928901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1141641, nsv1132737
SamplesKWS2, KWS1
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4057n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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